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Category:Laboratory & Technical Services

Compliance Assistant65161465063043120

Compliance Assistant

Summary: This role supports the compliance Partner Onboarding team by assisting with onboarding new partners and services, ensuring adherence to AML policies and regulatory requirements. Highlights: 1. Support compliance partner onboarding and network expansion 2. Conduct due diligence research and sanction screening 3. Contribute to creating new compliance policies and procedures **Description** Dandelion may be a new platform, but we’re not new to the industry. Backed by Euronet’s 35 years of experience in electronic payments, money transfers, and compliance, Dandelion is the largest, most diverse cross\-border payments platform, delivering real\-time payments across bank accounts, wallets, and cash. Today, our network spans more than 600,000 cash locations and over 4\.1 billion bank accounts and 3\.1 billion mobile wallets. We reach 170 countries around the world with over 90% of payments delivered in real\-time. **ABOUT THIS ROLE** **The main purpose of the role is to support the compliance Partner Onboarding team in the onboarding of new partners, services and expansions of the network as well as understanding the business to ensure compliance with our current AML Policies and procedures responsibilities and regulatory requirements.** **ROLES \& RESPONSIBILITIES** * Compliance due diligence and approval of New Partners globally * Review and approval of all expansion and service modifications related to Existing Partners, including: network expansions, business model expansions, or other modifications to the Partner Agreement. * Conduct due diligence research over available internal systems, the internet and other external data bases, including sanction screening and open\-source investigations. * When needed, assist with the on\-going due diligence process of existing Partners, including visits, KYC refresh and reporting. * Assist with the internal and external Audit management. * Contribute to creation of new policies and procedures, collaborating with supervisors and managers. **POSITION REQUIREMENTS** * Communication Skills * Strong research, analytical and reporting skills. * Excellent communications skills in English and Spanish, both oral and written. * Good planning and time management/prioritization skills. Ria Money Transfer offers a competitive salary and benefits package. **.** Actual compensation is based upon factors such as the candidate’s skills, qualifications, and experience. In addition, Ria Money Transfer offers a wide range of best in class, comprehensive and inclusive employee benefits for this role including healthcare, dental and vision benefits, Paid Vacation/ Sick Leave and more. Ria Money Transfer is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Check out our website to learn more about the company at: http://www.riamoneytransfer.com/ The position responsibilities outlined above are intended to define the general contents and requirements to perform this job. It is not to be taken as a complete statement of responsibilities or requirements. This job description does not restrict the Company’s right to assign or reassign duties and responsibilities to this job as needed.

C. Sol, 1, 28950 Moraleja de Enmedio, Madrid, Spain

Talent Sourcer (f/m/x)65156658960513121

Talent Sourcer (f/m/x)

Summary: Join AUTO1 Group's Country Operations Team as a Talent Sourcer to build strong talent pipelines through research and active sourcing for current and future staffing needs. Highlights: 1. Be part of an international Talent Sourcing Team on recruitment projects 2. Develop creative ideas for direct approach of specialists and executives 3. Grow and learn about sourcing tools and techniques to find great talents **Company Description** ----------------------- Join our Country Operations Team at AUTO1 Group as a Talent Sourcer. Your main responsibility will be to source talent and build a strong pipeline for current and future staffing needs. If you're interested in research and excited about recruiting, we want to meet you. AUTO1 Group is Europe’s leading digital automotive platform. We revolutionize the used car market with our well\-known brands **Autohero** , **wirkaufendeinauto.de** and **AUTO1\.com** . **Your new Role** ----------------- * Be part of our international Talent Sourcing Team and work on recruitment projects to find the best talents for the AUTO1 Group. * Develop creative ideas for the direct approach of specialists and executives \& become an expert for active sourcing. * Beyond the classic direct approach, you will regularly try out new tools and methods to identify interested candidates. * Be in charge of research projects and find innovative ways to attract and find candidates. * Ensure a strong talent pipeline for current and future staffing needs by building long\-lasting relationships with internal and external partners. **Your Skills** --------------- * A university degree in HR or in other related fields. * Experience in Talent Acquisition, sourcing or research. * Excellent communication skills in English. * Solutions and results oriented approach. * Fast\-adapting personality with a desire to grow and learn about sourcing tools and techniques to find great talents. **Our Offer** ------------- * Truly international (over 100 nationalities) and diverse working environment, transparency, clear communication and supportive, open\-minded team where you can be exactly who you are. * Our dynamic startup environment offers new challenges for personal growth with the contribution of own ideas. * Work remotely \- anywhere from Spain! * You get the chance to develop yourself personally and will be supported in achieving your goals through frequent feedback talks. * Flexible working hours. You will be able to adjust your daily journey around our core\-hours, making your start and end of the day compatible with your personal life. Join us, building the best way to buy and sell cars! You do not meet 100% of the requirements? Take your shot and apply anyway! We offer room for growth and challenges to learn from. Contact Anita Mare *At AUTO1 Group we live an open culture, believe in direct communication, and value diversity. We welcome every applicant; regardless of gender, ethnic origin, religion, age, sexual identity, disability, or any other non\-merit factor.* \#LI\-A1

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Senior CRA65156658720898122

Summary: This Senior Clinical Research Associate role involves overseeing and managing clinical trial activities to ensure protocol adherence, regulatory compliance, and data integrity. Highlights: 1. Oversee and manage clinical trial activities 2. Ensure data integrity, participant safety, and compliance 3. Monitor clinical trial sites and provide support Senior Clinical Research Associate Oncology Home based Spain ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. What You Will Be Doing:* Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. * Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. * Collaborating with cross\-functional teams to ensure timely and accurate data collection and reporting. * Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. * Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile:* Advanced degree in a relevant field such as life sciences, nursing, or medicine. * Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem\-solving skills. * Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools. * Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment. * Ability to travel at least 60% of the time (international and domestic \- fly and drive) and should possess a valid driver’s license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Field Quality Surveyor in Madrid65137708141953123

Field Quality Surveyor in Madrid

On-site Surveyor in the Central Area of Madrid. This is an extra assignment three times per month, always during morning hours. A work contract is offered. Knowledge of languages will be valued. Type of position: Permanent contract Work location: On-site employment

C. de la Abada, 6, Centro, 28013 Madrid, Spain

Food Safety and Quality Technician65137459057282124

Food Safety and Quality Technician

We are looking for an experienced food safety technician for a prestigious company in Madrid, Las Tablas area, in the collective catering sector. Your responsibilities will include maintaining the center's HACCP plan, attending internal and external audits, planning and monitoring corrective actions, training staff... A university degree in health sciences or food technology and a master's degree in food safety are required. We offer flexible working hours, meal allowances, and a pleasant work environment. Salary to be agreed upon. This position runs from February to October to cover a maternity leave. Interested candidates should contact us to schedule an interview. Job type: Full-time Benefits: * Meals at the company * Flexible working hours * Company laptop * Company phone Work location: On-site employment

C. del Arroyo de Valdebebas, 17, Hortaleza, 28050 Madrid, Spain

CRA II65137331928963125

Clinical Research Associate Home based Spain ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing* Conducting site qualification, initiation, monitoring, and close\-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. * Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing data review and resolution of queries to maintain high\-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile* Bachelor's degree in a scientific or healthcare\-related field. * Minimum of 2 years of experience as a Clinical Research Associate. * In\-depth knowledge of clinical trial processes, regulations, and ICH\-GCP guidelines. * Strong organizational and communication skills, with attention to detail. * Ability to work independently and collaboratively in a fast\-paced environment. * Ability to travel at least 60% of the time (international and domestic \- fly and drive) and should possess a valid driver’s license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Clinical Research Associate65137331911810126

Clinical Research Associate

Clinical Research Associate ICON plc is a world\-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. What you will be doing* Conducting site qualification, initiation, monitoring, and close\-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. * Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing data review and resolution of queries to maintain high\-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your profile* Bachelor's degree in a scientific or healthcare\-related field. * Minimum of 2 years of experience as a Clinical Research Associate. * In\-depth knowledge of clinical trial processes, regulations, and ICH\-GCP guidelines. * Strong organizational and communication skills, with attention to detail. * Ability to work independently and collaboratively in a fast\-paced environment. * Ability to travel at least 60% of the time (international and domestic \- fly and drive) and should possess a valid driver’s license What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well\-being and work life balance opportunities for you and your family. Our benefits examples include:* Various annual leave entitlements * A range of health insurance offerings to suit you and your family’s needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, TELUS Health, offering 24\-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well\-being. * Life assurance * Flexible country\-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion \& belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Medical Monitor (Gastroenterology)65137331878914127

Medical Monitor (Gastroenterology)

**Company Description** PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on\-time services across a variety of therapeutic indications. **Job Description** PSI **Medical Monitors** provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well\-being. **Responsibilities:** * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Advise clients, project teams, sites, regulatory agencies and third\-party vendors on medical matters * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments * Address safety issues across the trial from sites and the study team * Provide support for medical data review * Participate in bid defense meetings and proposal activities * Assist in Pharmacovigilance activities * Identify trial risks, and create and implement mitigation strategies with other relevant departments * Organize and lead clinical development advisory boards and safety monitoring boards * Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines **Qualifications** * Medical Doctor degree * Gastroenterology Fellowship certification is a must * Prior experience as a practicing MD (minimum of 10 years) * Prior research and/or industry experience is a plus * Full working proficiency in English * Proficiency with MS Office applications * Communication, presentation and analytical skills * Able to work in teams, problem\-solving, and detail\-oriented **Additional Information** As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Flight Test & Integration Engineer - COMMS / Datalink Systems65136966934401128

Flight Test & Integration Engineer - COMMS / Datalink Systems

Madrid Flight Test & Integration Engineer - COMMS / Datalink Systems Capgemini Engineering, a global leader in engineering services, brings together teams of engineers, scientists and architects to help the world’s most innovative companies unlock their potential and contribute to a better future. From autonomous vehicles to life-saving robots, our experts in digital technologies and software think outside the box, delivering unique R&D and engineering services across all industries. Join the team and advance your career at a company offering growth opportunities where you can make a difference—and no two days are ever the same! Are you passionate about the aerospace industry, tactical communication systems and working in test environments? At Capgemini Engineering, we are seeking a **Flight Test & Integration Engineer – COMMS / Datalink Systems** for a strategic aerospace sector project in Madrid. **What will you do in this role?** You will join the team responsible for **Flight Test Analysis**, laboratory testing and integration of communication systems (COMMS / Datalink). Your responsibilities will include: * Conducting **Lab Test Program Requirement Analysis**, including definition of test points, test conditions, database preparation and environment configuration. * Executing **integration tests** on **L2 and L1 rigs**. * Analyzing test data and participating in incident investigations **(snags/SARs)**. * Preparing **Lab Test Reports**, including the necessary technical analysis for their development. * Working with **Link 16/22 (TDMS)** protocols and test development, qualification and certification tools. * Collaborating with multidisciplinary teams in a highly technological environment focused on mission systems and datalinks. **What are we looking for?** * Degree in **Telecommunications**, **Electronics**, **Aeronautics**, **Industrial Engineering** or related field. * Knowledge of programming/scripting (highly desirable). * Experience or interest in communication system integration and testing. * Familiarity with laboratory environments, rigs and mission systems. * Prior experience with **TDMS / Link16 / Link22** is a plus. * **Technical English**. **Valued Skills** * System Testing * Integration Testing * Communication Systems * Navigation / Datalink * Flight Test Analysis * Programming & Scripting * Data Analysis * Laboratory Testing * L1/L2 Support Candidates holding a disability certificate will be positively considered within our inclusion and diversity policy. All applications are valued. We offer extensive training opportunities—both in-person and online—including certifications. Even if you don’t meet 100% of the desired qualifications, we’d love to meet you! Our commitment to inclusion and equal opportunity is reflected in our Equality Plan and Code of Ethics, which guarantee professional development for employees and equal opportunity in recruitment—within a discrimination-free environment based on ethnicity, nationality, social origin, age, sexual orientation, gender expression, religion or any other personal, physical or social circumstance. **What do we offer?** * A unique work environment highly rated by our professionals in periodic evaluations. * Wellbeing HUB: Includes policies and initiatives for physical health (Wellhub) and mental wellbeing. * 24 vacation days + 2 personal days + 24 and 31 December + option to purchase up to 7 additional vacation days per year. * FlexAbroad: possibility to work remotely from another country for up to 45 days. * Flexible Compensation Plan (medical insurance, transportation, training, meal card or food allowance, childcare…) * Continuous learning: access to Mylearning, Capgemini University, Digital Campuses and Professional Communities. You’ll also have access to platforms such as Coursera, Udemy, Pluralsight, Harvard Manager Mentor, Education First for languages (English, French, German…) and more! * Participation in Volunteering and Social Action initiatives through our Sustainability, Inclusion and Equality Groups. * Onboarding support through our Buddies program. * Life and Accident Insurance **Why choose us?** Capgemini is a global leader in transforming clients’ businesses by harnessing the full power of technology. Guided by our purpose—to create an inclusive and sustainable future through technology and the energy of those who build it—we are a responsible, diverse company and an international leader in IT and engineering services, with over 360,000 professionals across 50+ countries. With a strong 55-year heritage and deep industry expertise, clients trust Capgemini to address their full business needs—from strategy and design to operations—powered by the fast-evolving worlds of cloud, data, AI, connectivity, software, platforms and digital engineering. In 2022, the Group reported global revenues of €22 billion. Rewrite your future and **join the team!** #LI-CS21 Ref. code 393575-es_ES Posted on 18 Jan 2026 Experience level Experienced Professionals Contract type Permanent Location Madrid Business unit Engineering and R&D Services Brand Capgemini Engineering Professional communities Products & Systems Engineering

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Laboratory Technician65156659209859129

Laboratory Technician

Job Summary: We are seeking a Laboratory Technician to perform quality testing and analysis at the plant, ensuring the accuracy and reliability of results to meet high standards. Key Highlights: 1. Essential role in on-site quality testing and analysis 2. Responsible for rigorous control of laboratory documentation 3. Ensures compliance with high product quality standards We are looking for a Laboratory Technician in O Grove for a leading company in the canned food industry. Your role will be essential in conducting quality tests and analyses directly on-site, carefully recording all data obtained. You will be responsible for maintaining rigorous control over laboratory-generated documentation, ensuring analytical results are accurate and reliable. Your work will guarantee that the final product meets the highest quality standards required by our customers. A background in laboratory work and quality control is valued, as well as at least one year of prior experience in similar roles, preferably within the food industry. Shifts are rotating, Monday through Friday, covering mornings (07:00\-15:00h) and afternoons (15:00\-23:00h). * Education related to laboratory work and quality control. * At least one year of prior experience in the position, preferably in the food sector.

Rúa da Praza, 19, 36980 O Grove, Pontevedra, Spain

Associate Director, Patient Recruitment Strategy651060735132171210

Associate Director, Patient Recruitment Strategy

Madrid, Spain \| Full time \| Home\-based \| R1523996 **Be the strategic force behind patient‑centric trial success at IQVIA** At IQVIA, we are reimagining how clinical trials reach, engage, and support patients. Our Patient and Site Centric Solutions (PSCS) team partners with experts across the business to design strategies that help sponsors enroll and retain the right patients — while ensuring sites feel supported and empowered every step of the way. If you are passionate about improving the patient experience in research and want to influence global trial performance, this role offers a unique opportunity to make meaningful impact.**What you will do*** Develop and implement best‑in‑class patient recruitment, retention, and site‑engagement strategies to support customer enrollment goals. * Partner cross‑functionally to shape PSCS strategy both pre‑ and post‑award. * Lead elements of solution innovation to enhance our global recruitment and retention offerings. * Present strategy recommendations and insights during client bid‑defense meetings. * Create data‑driven budget estimates for proposed solutions. * Represent IQVIA at industry events, conferences, or webinars as a thought leader. * Collaborate with internal stakeholders to ensure all solutions meet quality and regulatory standards. * Mentor and coach team members to support development and team excellence. * Drive process improvement initiatives within PSCS. * Serve as a trusted liaison for internal teams and clients on recruitment strategy topics. **What you need to succeed*** Bachelor’s degree required. * 10\+ years of relevant experience, including 5\+ years in leadership roles. * Strong understanding of clinical development, patient recruitment, and site engagement. * In‑depth knowledge of GCP/ICH and applicable regulatory guidelines. * Demonstrated ability to analyze data and translate insights into effective strategies. * Solid understanding of clinical research financial parameters and budget management. * Excellent communication and presentation skills with the ability to influence stakeholders. * Strong leadership capabilities with a collaborative, relationship‑oriented style. * Proficiency in Microsoft PowerPoint, Excel, and Word. * Strong organizational and problem‑solving skills with the ability to manage competing priorities. **Why join IQVIA** At IQVIA, you’ll be part of a global team driving smarter healthcare for everyone, everywhere. You’ll work alongside innovators, clinicians, analysts, and strategists who are committed to improving patient outcomes and shaping the future of clinical development. Expect a culture built on collaboration, continuous learning, and opportunities for growth — supported by tools and insights that help you do your best work. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi\-talented collaboration harnesses innovation to deliver superior outcomes.

C/ de Juan Esplandiú, 11-13, Retiro, 28007 Madrid, Spain

Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)651060734845471211

Revenue Financial Controller - Laboratorio Central Health Diagnostics Quirónsalud (Alcobendas)

**At Quirónsalud, your career has a purpose.** At **Quirónsalud**, we do not just lead the healthcare sector; we are **transforming** it. With state-of-the-art technology and a network of over **58 hospitals in Spain and more than 180 healthcare centres across Europe**, backed by **Fresenius-Helios**, we work with a clear mission: **improving lives**. We are looking for professionals who want to **grow, innovate and be part of a team where excellence is part of everyday life.** **Join our team** **Position:** Revenue Financial Controller **Location:** Laboratorio Central Health Diagnostics (Alcobendas) **Key responsibilities:** * Lead the preparation of the annual revenue + activity budget and monitor its execution. * Monitor contracts and ensure correct tariff application. * Participate in defining and improving revenue and activity dashboards (KPIs_Power BI). * Contribute ideas and innovation to improve existing processes and systems. * Perform revenue closing and reconciliation with various profit centres and business units. * Prepare monthly and annual closing reports on revenue figures (billing/provisions/activity/KPIs). * Monitor monthly performance versus prior year and budget, analyse variances and propose improvements. * Monitor and evaluate profitability. * Analyse balance sheet accounts (revenue, bad debts). * Support audits. **What we offer:** * **Immediate onboarding** into a collaborative and specialised team. * **Attractive, competitive and market-aligned remuneration package.** * **An environment that fosters your development** * You will benefit from the support of an experienced team that will help you strengthen your skills and advance your career. * **Continuous training**: we will stimulate your learning and development through our **Quirónsalud University** and our **specific training plans**, enabling your personal and professional growth. **We care about your wellbeing** * **Access to our Health and Wellbeing Programme**, including initiatives such as: * + **Healthcare:** physical and mental wellbeing programmes (access to medical services, health maintenance programmes, psychological support). + **Financial wellbeing:** flexible compensation schemes, salary management facilities and exclusive discounts. + **Volunteering programme.** We’re waiting for you! *At Quirónsalud, we promote integration and respect for diversity. Therefore, our selection processes are conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that drive and foster equal treatment and opportunities between men and women, without discrimination—direct or indirect—based on gender. This principle forms part of our Corporate and People Policy, aligned with Organic Law 3/2007, of 22 March, on Effective Equality between Women and Men.* * Bachelor’s degree in Business Administration and Management (ADE), Economics, Business Studies, etc. * Minimum three years’ experience in similar roles. * Knowledge of SQL, Power Query, Power BI. * Proficiency in Excel. * Hospital or industrial sector experience is desirable.

Pl. Mayor, nº 1, 28100 Alcobendas, Madrid, Spain

Intern651060734667541212

**WHO WE ARE:** Plug and Play Tech Center is the ultimate innovation platform, bringing together the best startups and the world’s largest corporations to create the most meaningful connections that bring innovation to anyone, anywhere. We are on a mission to bring the benefits of Silicon Valley to all corners of the world. Each year, hundreds of entrepreneurs join our vertical\-specific accelerator programs to team up with our corporate members or receive a direct investment from Plug and Play. Plug and Play has over 45 locations across the world and our corporate members include: Daimler, Prologis, PG\&E, Nissan, Volvo, BP, Walmart, Nokia, Coca Cola, Doosan Bobcat, and over 500 more. Plug and Play’s corporate members utilize Plug and Play to identify the best startups to meet their challenges. Plug and Play’s proven investment track record includes Honey, Dropbox, Lending Club, Kustomer, Einride, and many more. **WHO WE’RE LOOKING FOR:** We’re an exceptional team with backgrounds in technology and entrepreneurship and we’re growing rapidly to deliver on our mission. We’re actively seeking an Intern to continuously deliver value to our partners under our fintech vertical in Madrid. An ideal candidate is highly strategic, ambitious, detail oriented, and able to effectively influence both within the organization and with our external partners. **HOW YOU’LL MAKE A DIFFERENCE:** As we live the startup spirit ourselves, no one in the team is exclusively limited to their main tasks. Rather, we are a dynamic team of all\-rounders who work closely together in all projects. However, your main role will be in supporting our team with the following tasks: Sourcing startups * Research and analyse the market and industry trends to identify the best early\-stage companies and founding teams with a specific focus. * Identify and reach out to promising startups. * Assist the senior team in evaluating startups from various sources. * Create meaningful and positive relationships with the startups and scale\-ups. Corporate facing * Coordinate the Plug and Play open\-innovation\-based deal flow and startup evaluation process together with our corporate partners. * Identify great startup offerings meeting corporate tech and business needs. * Funneling all individual interests of our corporate partners into the outline of the program and timeline (e.g. Workshops, Dealflow Sessions, Innovation Days, Demo Days etc.). * Introducing start\-ups to our corporate partners and helping our corporate partners engage with startups when there is a potential match or opportunity. Community Facing * Build and maintain an ecosystem of relevant stakeholders around innovation, venture capital and startups (incl. clusters, government representatives, universities, mentors, keynote speakers, etc.). Project \& Client Management * Support the end\-to\-end execution of open innovation programs, coordinating timelines, deliverables, and stakeholders across multiple projects. * Act as a day\-to\-day support point for corporate partners and startups, ensuring clear communication, follow\-ups, and alignment throughout the program lifecycle. * Track progress, prepare client\-facing materials, and contribute to continuous improvement of internal project management processes. **REQUIRED EXPERIENCE:** * Bachelor’s degree in Business Administration, engineering, economics or related field preferred. * Fluency in English and in Spanish is essential. * Detail oriented, highly organized, and comfortable working in a fast\-paced environment. * Strong process and analytical skills to identify inefficiencies and create improvements. * Excellent communication skills and proficiency in public speaking. * Passionate about technology with some background in the Startup ecosystem (research, courses, projects, etc…) * Project management and startup experience is a plus. * Ability to work with all levels of management is crucial. * Demonstrate integrity, responsibility, accountability, self\-awareness, work ethic, and empathy. * **All CVs must be submitted in English**

Calle de Lagasca, 37, Salamanca, 28001 Madrid, Spain

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology650936654097931213

Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology

Job Summary : Medpace is currently seeking candidates with **PhDs and/or Post\-Doctoral Research experience** for a full\-time, office\-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and **develop their career in the research and development of cutting\-edge therapeutics**. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Responsibilities : * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager * Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy * Compile and maintain project\-specific status reports within the clinical trial management system * Interact with the internal project team, Sponsor, study sites, and third\-party vendors * Manage and perform quality control of our internal regulatory filing system * Provide oversight and management of study supplies * Create and maintain project timelines * Coordinate project meetings and produce quality minutes Qualifications : * PhD in Life Sciences * Fluency in English with solid presentation skills * Ability to work in a fast\-paced dynamic industry within an international team * Prior experience within the CRO or pharmaceutical industry not required but will be advantageous Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

Senior Medical Writer - Sponsor dedicated - Remote role based in Europe650932765338911214

Senior Medical Writer - Sponsor dedicated - Remote role based in Europe

**Updated:** January 13, 2026 **Location:** Madrid, Spain **Job ID:** 25104394\-OTHLOC\-3529\-2DMAD\-2DR Not ready to apply? Join our Talent Network **Description** Senior Medical Writer \- Sponsor dedicated \- Remote role based in Europe Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments from the client. * Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports, clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. * Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved\-templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. * Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads team document reviews, and reviews documents as needed. * Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format. * Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. Provides feedback to further define statistical output required and document needs. * Interacts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables. * Performs online clinical literature searches and complies with copyright requirements. * Identifies and proposes solutions to resolve issues, escalating as appropriate. Provides technical support, training, and consultation to department and other company staff. May contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities. * Mentors and leads less experienced medical writers on complex projects, as necessary. * Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing. * Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership. * Completes required administrative tasks within the specified timeframes. * Performs other work\-related duties as assigned. * Minimal travel may be required (less than 25%). Qualifications: * 3\-5 years of relevant experience in science, technical, or medical writing. * Experience working in the biopharmaceutical, device, or contract research organization industry required. * Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required. * Experience writing relevant document types required. * Extensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within the Medical Writing job family are responsible for writing and editing manuscripts and other medical communications on clinical studies and/or scientific reports including special summaries from raw data for submission to regulatory agencies or for in\-company use, monographs, comprehensive reviews, scientific exhibits, and other projects requiring skill in medical communication such as screening, analyzing, and summarizing additional data from other sources as needed. Conducts systematic literature searches and reviews. Prepares literature for new products and revises existing medical communication. Reviews and analyzes statistical outputs to prepare results\-based documents such as clinical study reports and development safety update reports. Supports engagement and interaction with regulatory agencies through preparation of briefing books and response documents to health authority questions. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Individual contributor with developing subject matter expertise and responsibility for processes. In\-depth knowledge and skills within a professional discipline, understanding the impact of work on related areas. May be responsible for entire projects or processes within area of responsibility.

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Senior Epidemiologist (Oncology, Breast Cancer, RWE) - Sponsor Dedicated - Multiple Locations (home-based)650932764992011215

Senior Epidemiologist (Oncology, Breast Cancer, RWE) - Sponsor Dedicated - Multiple Locations (home-based)

Madrid, Spain \| Full time \| Home\-based \| R1523782**Job available in additional locations** *This is a home‑based position. Candidates can be located anywhere within one of the countries listed in the job ad.* *Candidates must have a permanent right to work in a country they apply for.* Join IQVIA’s Sponsor\-Dedicated FSP team and help advance healthcare through real\-world evidence. We bring together scientific expertise and real\-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise.**Overview:** Design and conduct epidemiological studies to generate real\-world evidence within time, budget, and quality standards, including but not limited to natural history of disease, population characterization, assessment of treatment patterns and unmet need, development of external comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research, and post\-authorization studies. Skill sets of the Epidemiologist role are similarly required, with the expectation of more experience, able to operate strategically under limited supervision, well versed in current Epidemiology research methods, deep understanding of how RWE fits within drug development, regulatory, medical, safety and other functions.**Responsibilities:*** Lead development of study protocols, analysis plans, and study reports to answer research questions of priority to RWE. * Lead, design, and manage epidemiological, biomarker and/or data science projects. * Lead, plan, design, and conduct analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries). * Lead the identification of fit\-for\-purpose data for the timely execution of the RWE strategy. * Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed. * Contribute to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers. * Support the effective communication of study/analysis results to support internal and external decisions. * Coauthor abstracts and manuscripts for external dissemination of methodologic study results. * Contribute to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities. * Technical Expertise: + Observational research methods (both Primary and Secondary), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes. o Ability to design studies independently, (i.e., ability to translate research questions to create study design). * Subject Matter Expertise: + Provide subject matter expertise and conduct analyses for descriptive and comparative research using RWD (examples include claims, EHR, PRO/COA, registry data) for methodologic research questions. + Lead the design and execution of post\-marketing and observational safety studies to evaluate product risk profiles and inform regulatory and clinical decision\-making. + Contribute to engagements with regulatory authorities to provide scientific input, respond to safety\-related inquiries, and ensure compliance with evolving regulatory requirements. **Requirements:*** **PhD in Epidemiology with a minimum of four (4\) years of post\-doctoral experience, preferably at a pharmaceutical company. Master’s degree in Epidemiology plus 7\-9 years of experience in lieu of PhD may be acceptable.** * **Oncology Specific: expert knowledge and extensive experience (at least 2\+ years leading studies) with cancer epi (solid tumor experience a plus), extensive experience with oncology EMR databases, extensive experience with conducting cancer epi studies.** * **Pharmaco Epidemiology Specific: expert knowledge and extensive experience with pharmacoepi methods (i.e., signal detection and validation methods), expert understanding of regulatory requirements for safety reporting and analysis, RMPs, and PASS both US and global.** * Deep understanding of observational research methods and experience to support the design and conduct of observational research, including protocol, statistical analysis plan, and study report development. * Extensive knowledge of secondary data sources and experience with secondary data analysis, including electronic medical record and/or medical claims databases. * A record of scientific publications demonstrating expertise in observational study design, analysis, and interpretation is preferred. * Demonstrated ability to function with an increasing level of autonomy and to develop productive cross\- functional collaborations in a matrix environment. * Ability to manage priorities and performance targets. **What’s in it for you?*** Be part of a forward\-thinking team that helps shape the next generation of evidence\-based healthcare. * Work hand\-in\-hand with one leading sponsor, gaining deep expertise in their therapies. * Access IQVIA’s global network who supports your growth. This is your chance to make an impact, while building a career that matters. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

C/ de Juan Esplandiú, 11-13, Retiro, 28007 Madrid, Spain

Data Analyst Researcher650854636096031216

Data Analyst Researcher

**Our client:** One of the leading NGOs dedicated to helping children and adolescents at risk, with a unique project in Spain. **Job description:** * Collect, summarize, and analyze documents and statistics for various studies and research projects. * Prepare reports and monographic studies, conducting qualitative and quantitative analyses to ensure appropriate data processing and identify trends. * Carry out sample design. * Develop information collection tools: questionnaires, interview scripts, focus group discussion guides, codebooks, etc. * Code information, tabulate data, and prepare statistics and charts for results reports. * Draft results reports and deliver presentations to disseminate findings. * Develop databases. **Requirements:** * University degree in Sociology, Statistics, or related fields in research. * Minimum 3 years’ experience in data and research-related areas or in similar positions. * Advanced Excel skills (functions, formulas, pivot tables and charts, at minimum). * Advanced proficiency in statistical software (SPSS). * Minimum English language level B2. * Proficiency in tools such as Atlas.ti or SurveyMonkey will be valued. **We offer:** * Training and opportunities for professional growth. * Permanent contract. * Competitive salary according to experience. * Working hours: Monday to Thursday, 9 a.m. to 6 p.m.; Friday, 9 a.m. to 3 p.m.

C. de la Abada, 6, Centro, 28013 Madrid, Spain

Intensivist Physician650854635470091217

Intensivist Physician

**Quirónsalud** --------------- Quirónsalud is the leading healthcare services provider in Spain. We count on internationally renowned experts in the biomedical field and a large team of healthcare and non-healthcare professionals who work day in and day out to deliver the highest quality specialized care in our country. At Quirónsalud, we seek the best professional talent to continue offering distinctive healthcare services distinguished by their quality, high level of specialization, and person-to-person health care. **Job Description** ---------------------------- At Quirónsalud, we not only lead the healthcare sector—we are transforming it. Backed by Fresenius-Helios, with state-of-the-art technology and a network of over 58 hospitals across Spain and more than 180 healthcare centers throughout Europe, we operate with a clear mission: improving lives. We are looking for professionals who wish to grow, innovate, and become part of a team where excellence is part of everyday life. From Quirónsalud’s private hospitals in Madrid, we are seeking an Intensivist Physician to join the Ruber Juan Bravo University Hospital, located in central Madrid. **Join Our Team** **Position:** Intensivist Physician. **Location:** Ruber Juan Bravo University Hospital. **What We Offer:** * Immediate integration into a collaborative and specialized team. * Option to work at 50% or 100% capacity. * Indefinite-term employment contract. Possibility of entering into a commercial contract. * Flexible working hours under all contract types. Shifts of 24, 15, or 17 hours on call are available, as well as 7-hour reinforcement shifts. * Competitive remuneration aligned with current offerings in the private healthcare sector in the Community of Madrid. * Opportunity to participate in research projects and paid teaching activities. * A hospital and service philosophy grounded in teamwork, quality patient care, and a positive working environment. * Becoming part of the Quirónsalud Group, the national leader in the healthcare sector. **An Environment That Enhances Your Development** * You will benefit from the support of an experienced team that will help you strengthen your skills and advance your career. * Continuous training: we will foster your learning and development through Quirónsalud University and our specific training programs, enabling both personal and professional growth. **We Care About Your Well-being** * Access to our Health and Well-being Program, which includes initiatives such as: + Health care: physical and mental well-being plans (access to medical services, health maintenance programs, and psychological support). + Financial wellness: flexible compensation programs, salary management assistance, and exclusive discounts. + Family care: initiatives focused on promoting healthy lifestyles and work-life balance. + Volunteering program. We’re waiting for you! *At Quirónsalud, we promote inclusion and respect for diversity. Therefore, our selection processes are conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that foster and encourage equal treatment and opportunities between men and women, without direct or indirect discrimination based on gender. This principle forms part of our Corporate and People Policy, in line with Organic Law 3/2007, of March 22, on Effective Equality Between Women and Men.* **Requirements** -------------- * Degree in Medicine (official recognition and work permit required for non-EU professionals). * Specialty in Intensive Care Medicine via the MIR program. * Professional experience and additional continuous training will be valued. Do you already have a profile on ? Autocomplete with b4work **Position:** FACULTATIVO**Department:** QS-FACULTATIVO**Location:** Madrid (Spain)**Working Hours:** Full-time**Sector:** Health**Vacancies:** 1**Discipline:** Others**Work Modality:** On-site

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Brand Campaign Specialist

Who we are We are on a mission to make all science open, enabling the research community to develop the solutions we all need to live healthy lives on a healthy planet. Frontiers is one of the world’s largest and most impactful research publishers, dedicated to making peer\-reviewed, quality\-certified science openly accessible. Our articles have been viewed 4 billion times, reflecting the power of research that is open for all. Follow the links below to learn more about our work. www.frontiersin.org/about/annual\-reports www.youtube.com/watch?v\=87ejFfnQzko What we can offer you At Frontiers, our working model for new roles includes a balanced approach that fosters collaboration through regular engagement at our office hubs in key locations. While we value flexibility, we also believe that shared in\-person time strengthens team culture, trust, and productivity. We provide a range of benefits across our global locations, including but not limited to:* 4 additional wellbeing days in addition to existing annual leave allowance * Access to learning platforms and dedicated learning \& development time * A range of wellbeing initiatives, including free online yoga classes and an employee assistance plan * Employees can dedicate three days each year to volunteer * Additional benefits depending on your location (e.g. pension plan and private medical care) The role The Brand Communications and Campaigns Specialist develops, delivers, and elevates brand\-led communications across Frontiers. This role shapes and executes integrated campaigns—defining clear messaging, creating compelling content, and ensuring consistent storytelling across channels—to bring our brand story, values, and strategic priorities to life. Working closely with colleagues across Digital Marketing, Editorial, Research Integrity, Design, Internal Communications, and leadership, the Brand Communications and Campaigns Specialist ensures strong brand expression and impactful storytelling across campaigns, platforms, and audiences. This is a hands\-on, creative, and strategic role for someone who thrives on turning complex ideas into engaging narratives—and delivering polished, on\-brand communications at pace. Key responsibilities:* Develop and implement brand communications campaigns that highlight Frontiers’ mission, editorial model, technologies, and impact. * Plan and execute messaging frameworks and narrative structures for campaigns and strategic initiatives, ensuring alignment with brand strategy and organizational priorities. * Produce high\-quality content across various formats—such as campaign copy, video scripts, social and web copy, leadership messaging, blog posts, and infographics—translating complex topics into clear, accessible storytelling. * Collaborate with in\-house teams to create multimedia content and ensure brand consistency across all communications and assets. * Support the rollout and evolution of brand guidelines, toolkits, and templates for internal use. * Work cross\-functionally with publishing, editorial, digital marketing, and product teams to articulate differentiating stories and meet communications needs for events, campaigns, product launches, and organizational announcements. * Respond quickly to emerging communication needs and contribute to special projects such as annual reports, editorial series, leadership speeches, and brand campaigns. Requirements: Essential:* Experience in brand, communications, marketing, or content development\- ideally within publishing, science, technology, academia, or mission\-driven organizations. * Exceptional writing and editing skills, with a proven ability to craft compelling narratives. * Ability to distil complex information into accessible messaging. * Experience developing campaign messaging and multi\-channel content. * Strong organizational skills and the ability to manage multiple projects and stakeholders simultaneously. * A collaborative approach and comfort working with specialists from diverse disciplines. Desirable:* Understanding of open science, research publishing, academic communication, or scientific storytelling. * Experience in video scripting, brand messaging frameworks, or brand governance. * Familiarity with working in a fast\-paced, global environment. * Experience using web and email content management systems Why to join our team?* The opportunity to shape and elevate the communications of a global leader in open science. * A mission\-driven culture focused on research integrity, scientific advancement, and societal benefit. * Collaboration with international teams across brand, editorial, technology, and marketing. * Professional growth in a creative, innovative, and purpose\-led communications function. Apply now Please click the 'apply' button on this page and submit your application in English. Please inform us if you require any special accommodations to participate fully in our recruitment experience. You can contact us at careers@frontiersin.org for any additional support. *Equal opportunity statement* *Frontiers actively embraces diversity and is a safe and welcoming workplace. Recruitment is free from discrimination – including based on race, national or ethnic origin, age, religion, disability, sex, gender identity or sexual orientation. With employees from more than 50 different nations, our diversity creates vibrant teams and constantly challenges us to appreciate multiple perspectives.*

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Postdoctoral researcher in electroactive biomaterials and medical devices650854634976011219

Postdoctoral researcher in electroactive biomaterials and medical devices

Design and additive manufacturing of biomaterials and medical devices using electroactive materials **OTHER DETAILS** **Ref. num.** 2026\-AD\-R2\-312 #### **Postdoctoral researcher in electroactive biomaterials and medical devices** IMDEA Materials Institute is a public research organization founded in 2007 by Madrid’s regional government to carry out research of excellence in Material Science and Engineering by attracting talent from all over the world to work in an international and multidisciplinary environment. IMDEA Materials has grown rapidly since its foundation and currently includes more than 120 researchers from 22 nationalities and has become one of the leading research centers in materials in Europe which has received the María de Maeztu seal of excellence from the Spanish government. The research activities have been focused on the areas of materials for transport, energy, and health care and the Institute has state\-of\-the\-art facilities for processing, characterization and simulation of advanced materials. **Description** The researcher will work within IMDEA Materials’ research line on *“Bioinspired, Smart, and Living Materials”*, focusing on the design and additive manufacturing of biomaterials and medical devices using electroactive materials. The main research tasks will include the design, computational modeling, additive manufacturing, and testing of advanced medical devices based on active or multifunctional materials, particularly polymer‑matrix electromagnetic composites and shape‑memory alloys from the nitinol (Ni‑Ti) family. The researcher will collaborate in the development and testing of prototypes of structures and medical device concepts based on these material families, combining fused filament fabrication and laser powder bed fusion. The researcher will work with the research line team on dissemination, communication, and project proposal preparation activities, as well as on documenting the research carried out. The researcher will contribute to IMDEA Materials Institute’s strategic initiatives, especially those related to open science and innovation, and will work actively with other teams in the institute, particularly within the advanced manufacturing program and the materials for health research line. **Requirements** Industrial, mechanical, electronics or materials engineering master's degree with a PhD in the field of additive manufacturing, if possible connected to the printing of electromagnetic\-responsive materials. Expertise with computational modeling (CAD and FEM simulations), use of common 3D printing slicers and rapid prototyping, including electronics prototyping. Evaluation will be based on 1\) Curriculum vitae, 2\) Motivation letter, 3\) Research portfolio (background summarized as a presentation with highlighted achievements, 4\) selection of up to 3 scientific publications. Candidates not submitting the required documents will be discarded. **Conditions** The position opens for a trial period of 6 months until additional funding is secured from already presented project proposals and ongoing and forthcoming competitive research calls. Proposed start date is February 16th 2026\. Applications are processed upon reception. The position might be closed once ten working days have passed since publication, so **we encourage early application.** The working language of the Institute is English. Full command of the English language is required in all positions. **WHAT YOU WILL FIND AT IMDEA**: Stimulating environment where you can grow professionally. IMDEA Materials Institute is committed to equal opportunities, diversity and the promotion of a healthy work environment and work\-life balance. **Female applicants are encouraged to apply** to our research and technical positions. Besides on\-the\-job technical training, IMDEA Materials Institute is committed to training the Institute’s scientists and staff in “soft” or transversal skills

C. Cuestas Bajas, 12A, 28901 Getafe, Madrid, Spain

Systems Communications Integration Engineer (Junior)650849059674891220

Systems Communications Integration Engineer (Junior)

Madrid Systems Communications Integration Engineer (Junior) **Capgemini Engineering**, a global leader in engineering services, brings together teams of engineering, science, and technology professionals to help the world’s most innovative companies unlock their potential and contribute to a better future. From autonomous vehicles to life-saving robots, our digital technologies and software experts think outside the box, delivering unique R\+D and engineering services across all industry sectors. Join the team and advance your career at a company offering growth opportunities—where you can make a difference and no two days are ever the same! . **About the Role** Capgemini Engineering is seeking a Systems Communications Integration Engineer (Junior) to join our team and participate in the integration and testing of tactical communications systems. If you’re passionate about aerospace, mission systems, and laboratory environments, this opportunity is for you! . **What You’ll Do on the Project?** * Prepare and execute tests on integration benches (rigs). * Analyze test results and support incident investigation. * Create technical documentation and test reports. * Collaborate with multidisciplinary teams in a highly technological environment. . **Your Profile** To thrive in this role, you should have: * An engineering degree (Telecommunications, Electronics, Computer Science or related field). * Minimum 1 year of experience in testing, communications, or systems environments. * Basic programming/scripting skills (Python, TCL, etc.). * Interest in aerospace and communications systems. * English language proficiency at B2 level. . Holding a disability certificate will be positively considered within our inclusion and diversity policy. We value all applications. We offer extensive training programs and certification opportunities. Even if you don’t meet 100% of the requirements, we’d love to meet you! **What You’ll Love About Working Here** . We offer a flexible environment with growth opportunities: * A uniquely valued workplace, consistently rated highly by our professionals in periodic evaluations. * Wellbeing HUB — Includes policies and initiatives supporting physical health (Wellhub) and mental well-being. * 24 vacation days \+ 2 personal days \+ December 24 and 31 \+ option to purchase up to 7 additional vacation days per year. * FlexAbroad: possibility to work remotely from another country for up to 45 days. * Flexible Compensation Plan (health insurance, transportation, training, meal card or food allowance, childcare, etc.). * Continuous learning: access to MyLearning, Capgemini University, Digital Campuses, and Professional Communities. Platforms include Coursera, Udemy, Pluralsight, Harvard Manager Mentor, Education First for languages (English, French, German, etc.)—and more! * Participation in Volunteering and Social Action initiatives through our Sustainability, Inclusion, and Equality Groups. * Onboarding support through our Buddy Program. * Life and Accident Insurance. . **Why Capgemini Engineering?** . Capgemini is a global leader in digital transformation and business management, driving an inclusive and sustainable future through technology. We employ over 360,000 professionals across 50+ countries. Our commitment to equal opportunity is reflected in our Equality Plan and Code of Ethics, ensuring a discrimination-free environment—regardless of origin, ethnicity, nationality, gender, age, sexual orientation, gender identity, religion, or any other personal or social circumstance. . **Rewrite Your Future. Join Capgemini Engineering!** Apply now at www.capgemini.com/es\-es \#LI\-AR13 Ref. code 366948\-es\_ES Posted on 14 Jan 2026 Experience level Experienced Professionals Contract type Permanent Location Madrid Business unit Engineering and R&D Services Brand Capgemini Engineering Professional communities Products \& Systems Engineering

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Cosmetic Laboratory Quality Control Technician650600308089611221

Cosmetic Laboratory Quality Control Technician

We are looking for you as: **Cosmetic Laboratory Quality Control Technician** ================================================= **Location** Madrid **Contract Type** Temporary\+Indefinite **Start Date** Immediate International leading company in the cosmetic industry, headquartered in Arganda del Rey. We specialize in the manufacturing and production of skin and hair care products in liquid and wipe formats. We need to hire a person for the Technical and Quality Control area. **Requirements:** --------------- * Higher Technician in Laboratory Analysis and Quality Control or equivalent * Experience in cosmetic laboratories * Experience in physicochemical analysis **Job Description:** --------------------------- * Raw material, semi-finished product and finished product analysis * pH, density, viscosity and refractive index analysis * Issuance and transcription of test reports * Sampling, analysis and issuance of test reports * Conducting attribute-based inspection controls **What we offer you:** --------------------- * Development and growth opportunities * Salary according to merit * Working hours: Monday to Friday, rotating shifts from 06:00 to 14:00 / 14:00 to 22:00 / 22:00 to 06:00 * Work location: Arganda del Rey. ### **Got more questions?** If you have any doubts, contact us at phone number 91 871 41 50 ### **Address** Calle Álava, 5 28500 \- Arganda del Rey

C. Álava, 5, 28500 Arganda del Rey, Madrid, Spain

Clinical Research Physician650493813260811222

Clinical Research Physician

Job Summary : We are seeking Clinical Research Physicians to join our dynamic team. The Clinical Research Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Clinical Research Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Clinical Research Physicians in the following Therapeutic Areas: * Psychiatry * Pediatric / Neuromuscular Neurology * GI / Hepatology * Dermatology * Metabolic / Endocrinology \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Must have prior clinical trial research experience; and * Previous experience in pharmaceutical\-related clinical research is preferred. **Travel**: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

Pediatric / Neuromuscular Neurologist650493813096981223

Pediatric / Neuromuscular Neurologist

Job Summary : We are seeking a Pediatric / Neuromuscular Neurologist to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

Hepatology - Medical Director650493812925471224

Hepatology - Medical Director

Job Summary : We are seeking a Hepatologist to join our team in London. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. \*\*All Medical Monitors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

Psychiatry - Medical Director650493812759071225

Psychiatry - Medical Director

Job Summary : We are seeking a Psichiatry Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

Dermatologist - Medical Director650493812591371226

Dermatologist - Medical Director

Job Summary : We are seeking an Dermatologist \- Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. \*\*All Medical Directors have hybrid WFH flexibility. Responsibilities : * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Participate in new business development through involvement in proposal and sponsor meetings as requested; * Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents; * Follow specific research related protocol and lead others in strict adherence to the policies. Qualifications : * Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical\-related clinical research is preferred. Travel: up to 20% Medpace Overview : Medpace is a full\-service clinical contract research organization (CRO). We provide Phase I\-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti\-viral and anti\-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40\+ countries. Why Medpace? : People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30\+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. **Medpace Perks** * Flexible work environment * Competitive compensation and benefits package * Competitive PTO packages * Structured career paths with opportunities for professional growth * Company\-sponsored employee appreciation events * Employee health and wellness initiatives **Awards*** Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility **What to Expect Next** A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

C. de Santiago Bernabéu, 12, Chamartín, 28036 Madrid, Spain

Personal warehouse laboratory650493701854751227

Personal warehouse laboratory

Warehouse assistant sought for a major pharmaceutical laboratory in Meco. The position focuses on the distribution area, where the candidate will actively participate in organizing and ensuring the smooth operation of the warehouse. Main responsibilities include ensuring compliance with the laboratory's quality standards, as well as performing cleaning and maintenance tasks for the facility. The candidate will also be responsible for order preparation, including labeling and strapping, and will maintain thorough documentation of delivery notes, managing goods receipts and dispatches. A substitution contract is offered with a fixed night shift, Monday to Friday, from 23:00 to 07:00 hours. **Requirements:** * Minimum education level: high school diploma, vocational training level 1 (FP1), vocational training level 2 (FP2) or higher (the relevant diploma/certificate of grades will be requested; official recognition/homologation is not required). * Minimum 1 year of experience as a warehouse assistant in the pharmaceutical or food sector (preferably). * The job involves a high physical workload.

C. Reino Unido, 7, 28880 Meco, Madrid, Spain

Researcher (fluent Arabic and Kurdish)650493700788511228

Researcher (fluent Arabic and Kurdish)

**Role Purpose** The aim of compliance\-driven due diligence is to assess our clients’ actual or potential counterparties, looking for any issues that might pose a reputational or other risk to them. As part of a dedicated team (VANTAGE), the compliance due diligence researcher role involves media research, working with databases, primary documents and other sources to uncover reputational and criminal issues and ultimate beneficial ownership, as well as making sense of complex corporate structures and identifying possible political and sanctions exposure. Your main task will be to review, coordinate and report the findings of OSINT and HUMINT research concisely within short timeframes. A meticulous eye for detail is a must in this challenging, fast\-paced role. The right candidate will be a team player who can maintain a positive attitude under pressure. You will be required to make sense of complex information and have a clear and crisp writing style. **What you'll do:** * Work on a range of due diligence assignments, which include corporate compliance/ABAC/ESG and financial crime/IPO/KYC projects * Conduct media and database research using complex search criteria and following a strict methodology * Liaise with in\-country source networks to obtain relevant compliance\-related information not available via OSINT sources. * Analyse search results within the context of the project and the country, * Distil conclusions and identify indirect connections from research findings * Rate findings based on standard or tailored risk assessment methodologies * Summarise all relevant findings in a report * When required, brief and present findings to internal colleagues * Collaborate with team members across the firm to deliver joint projects **Requirements** **Essential** * Knowledge of research techniques, databases, networks, online registers and archives, and research in the general internet * Knowledge of the business, political, and social context of a geographical area * **Native or equivalent fluency in English and Arabic and Kurdish** * Excellence in research and writing in English and clear communication style * Communicate complex topics verbally and in writing effectively * Ability to summarise large amounts of information in a clear and concise manner * Ability to manage and prioritise multiple tasks to tight deadlines * Curiosity, attention to detail and problem\-solving skills * Ability to work independently and in a team * Education to degree level **Preferred** * Demonstrated professional experience * Fluency in an additional language **Benefits** * Control Risks offers a competitively positioned compensation and benefits package that is transparent and summarised in the full job offer. * We operate a discretionary global bonus scheme that incentivises, and rewards individuals based on company and individual performance. * Control Risks supports hybrid working arrangements, wherever possible, that emphasise the value of in\-person time together \- in the office and with our clients \- while continuing to support flexible and remote working. * Working with our clients, from day one our people are given direct responsibility, career development and the opportunity to work collaboratively on fascinating projects in a rewarding and inclusive global environment. * The Company is committed to further its diversity, inclusion and equity agenda and as an employee you have access to various business resource groups in the Company including the Company's LGBT\+ network called MOSAIC, the Women's Network, and Synergy \- a people network to celebrate and promote ethnic diversity at Control Risks *Control Risks is committed to a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age or veteran status”* *If you require any reasonable adjustments to be made in order to participate fully in the interview process, please let us know and we will be happy to accommodate your needs.*

Prta del Sol, 4, 2ºC, Centro, 28013 Madrid, Spain

Research assistant (Predoctoral researcher) for developing new generation fire-safe storage energy materials and advanced composites650493700476181229

Research assistant (Predoctoral researcher) for developing new generation fire-safe storage energy materials and advanced composites

The researcher will mainly focus on designing and preparing new generation eco\-friendly fire\-safe strategies for energy storage materials and exploring their advanced applications, and will study at the high\-performance polymer nanocomposites group http://www.materials.imdea.org/groups/hppn/ at IMDEA. **OTHER DETAILS** **Ref. num.** 2026\-DW\-R1\-310 #### **Research assistant (Predoctoral researcher) for developing new generation fire\-safe storage energy materials and advanced composites** IMDEA Materials Institute is a public research organization founded in 2007 by Madrid’s regional government to carry out research of excellence in Material Science and Engineering by attracting talent from all over the world to work in an international and multidisciplinary environment. IMDEA Materials has grown rapidly since its foundation and currently includes more than 120 researchers from 22 nationalities and has become one of the leading research centers in materials in Europe which has received the María de Maeztu seal of excellence from the Spanish government. The research activities have been focused on the areas of materials for transport, energy, and health care and the Institute has state\-of\-the\-art facilities for processing, characterization and simulation of advanced materials. **Description** In this study, the student will mainly focus on studying new generation fire\-safe energy storage materials, such as fire\-safe Lithium\-ion batteries, supercapacitors, etc. In detail, the main research tasks include: * Development of high efficient eco\-friendly fire\-safe strategies to energy storage materials * Investigation of fire\-safe composites for battery housing system * In\-depth understanding of the underlying mechanisms The candidate will acquire hands\-on experience with energy storage materials. The candidate will gain experience in fundamental and applied research in materials science, engineering, and high\-performance polymers, opening perspectives in academia and industry. **Requirements** Candidate should hold a master’s degree in chemistry or Materials Science and Engineering or a related field/discipline and a strong commitment to developing scientific activity in an international and multidisciplinary environment. Fluent English (written and oral) is needed. Previous experience in battery or energy storage materials will be highly appreciated and positively evaluated. **Conditions** Interested candidates are encouraged to apply as soon as possible to ensure the best consideration of their application. Screening of candidates will begin immediately. The first contract is for 12 months and will be extended after passing the evaluation. Online Application deadline: 09 Feb 2026\. Applications are processed upon reception. The position might be closed once ten working days have passed since publication, so **we encourage early application.** The working language of the Institute is English. Full command of the English language is required in all positions. Applications are processed upon reception. The position might be closed once ten working days have passed since publication, so **we encourage early application.** The working language of the Institute is English. Full command of the English language is required in all positions. **WHAT YOU WILL FIND AT IMDEA**: Stimulating environment where you can grow professionally. IMDEA Materials Institute is committed to equal opportunities, diversity and the promotion of a healthy work environment and work\-life balance. **Female applicants are encouraged to apply** to our research and technical positions. Besides on\-the\-job technical training, IMDEA Materials Institute is committed to training the Institute’s scientists and staff in “soft” or transversal skills

C. Cuestas Bajas, 12A, 28901 Getafe, Madrid, Spain

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