Yuncos Laboratory & Technical Services Job Listings

Social Research Technician at Headquarters

Country Spain Province Madrid – Madrid Application Deadline 28/12/2025 Category Project Management Type of Offer Targeted at persons with disabilities **Create alert** **Information about the NGO** ACCEM, Association **Rating** (1 rating) **info** Response rate: 69.86% **info** **Objective** ------------ We are a non-profit, non-partisan, and non-denominational organization working to improve the living conditions of people in situations of vulnerability. We uphold equality of rights, duties, and opportunities for all individuals, regardless of their racial or ethnic origin, sex, nationality, sexual orientation or gender identity, religion, opinion, or social group affiliation. Currently, we are seeking a Social Research Technician at our headquarters (Madrid). Responsibilities: * Analysis of statistical sources and literature review * Design of tools for data collection: interview scripts, focus groups and participatory workshops, field diaries, records of virtual ethnographies, evaluation forms, facilitation sheets, etc. * Recruitment of study participants and contact with key informants * Planning and management of fieldwork * Application of qualitative and ethnographic techniques: qualitative interviews, focus groups, participatory workshops, observations, virtual ethnographies, evaluation forms * Transcription of interviews * Qualitative discourse and content analysis * Application of gender and intersectional approaches in analyses * Development of materials presenting study conclusions * Drafting of final reports for publication * Organization of the event presenting study results * Public and media presentations of study findings * Preparation of technical monitoring and program justification reports * Document preparation and organizational support * Other activities related to programs Offer includes: * Indefinite-term contract * Full-time schedule, Monday to Friday, either from 08:00 to 15:00 or from 09:00 to 16:00. * Possibility of teleworking 3 days per week. * Annual gross salary: €25.518. **Profile:** * University degree in Sociology or Anthropology. * At least 1 year’s experience as a qualitative social research technician. * Active participation in all project phases. * Ability to handle large volumes of information. * Experience collaborating with other organizations in networked work. * Knowledge of discrimination and racism. * Analytical, interpretive, and synthetic capacity. * Familiarity with the social sector, particularly migration-related issues. * Strong oral and written communication skills. * Experience drafting materials and reports. * Reliability in meeting established deadlines. * Teamwork skills. * Language proficiency is desirable. * Knowledge of MySQL and R is desirable. **Competencies:** Problem analysis and resolution, Initiative and autonomy, Capacity for learning, Ability to lead initiatives, Organization and planning, Technical and personal reliability, Interpersonal communication, Teamwork **Level:** Employee **Type of contract:** Full-time **Duration:** Indefinite **Salary:** Between €24,001 and €30,000 gross/year **Minimum education:** Diploma **Minimum experience:** At least 1 year **Start date:** 11/12/2025 **Number of vacancies:** 1

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

€ 24,001-30,000/year

Researcher (fluent Italian)64706870969987121

Indeed

Researcher (fluent Italian)

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 Italian** + 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 + Additional fluency in another European 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. * As an equal opportunities employer, we encourage suitably qualified applicants from a wide range of backgrounds to apply and join us and are fully committed to equal treatment, free from discrimination, of all candidates throughout our recruitment process. Apply for this job

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

Negotiable Salary

International Project Manager64732464538113122

Indeed

International Project Manager

UNIR, a leading university in online education, is seeking talented individuals to join its team in the field of international project management. If you are passionate about university education and its innovation through technology, this is your opportunity. Join an institution experiencing robust growth and international expansion, comprising over 5,000 professionals and boasting more than ten years of experience—making it a benchmark for Spanish-language online higher education. UNIR’s **Vice-Rectorate for International Projects**, recognizing the importance of research activity for our faculty, our university, and society, promotes, develops, and coordinates UNIR’s overall research policy. To channel and facilitate faculty research activities, it designs and manages initiatives aimed at strengthening UNIR’s presence in competitive international research project calls. The primary objective is to increase scientific output, participation in national and international projects, and research transfer activities. UNIR places special emphasis on developing research collaborations with other countries, convinced that an extensive network of relationships, agreements, and joint activities brings significant benefits to all participants. Within this context, we seek to hire an **International Project Manager**, responsible for advising various faculties—from administrative support and proposal submission procedures to final reporting and justification of approved projects. **Responsibilities** * Management of R&D projects and advisory services to various faculties. * Participation in drafting international R&D project proposals. * Coordination of development tasks within R&D&i project frameworks. * Teamwork with international partners. * Documentation and justification of tasks. * Ensuring compliance with work plans, deliverables, reporting requirements, and commitments established in grant awards and/or contracts. **Requirements** * Demonstrable experience of at least three years in R&D&i project management (e.g., Erasmus+, Horizon Europe, MinCiencias, IDRC, etc.). * Involvement in all project phases (negotiation, contracting, reporting, etc.). * Advanced level of English. **Competencies** * Planning and organization, teamwork, flexibility, and effective communication. *Universidad Internacional de La Rioja, S.A.U. (hereinafter, "UNIR"), as a member entity of the PROEDUCA Group, will process the personal data you have provided for the following purposes: managing your participation in recruitment processes, evaluating your profile, and, if suitable for other vacancies, sharing it with other companies within the Group.* *Detailed information regarding the processing of your personal data is available in the legal text accompanying the application form. You may withdraw your consent and exercise the rights granted under Articles 15 to 22 of Regulation (EU) 2016/679 by submitting a request to Av. de la Paz, 137, 26006 Logroño, or via email to* *ppd@unir.net**, clearly identifying yourself. If desired, additional and detailed information on data protection is available at the following* *link**.* * *The EDUCATIONAL GROUP is firmly committed to equal opportunities and diversity, thereby fostering an environment free from any form of discrimination.*

C. de García Martín, 16, 28224 Pozuelo de Alarcón, Madrid, Spain

Negotiable Salary

Director - Strategy and Integration64749999694465123

Indeed

Director - Strategy and Integration

Expedia Group brands power global travel for everyone, everywhere. We design cutting\-edge tech to make travel smoother and more memorable, and we create groundbreaking solutions for our partners. Our diverse, vibrant, and welcoming community is essential in driving our success. **Why Join Us?** To shape the future of travel, people must come first. Guided by our Values and Leadership Agreements, we foster an open culture where everyone belongs, differences are celebrated and know that when one of us wins, we all win. We provide a full benefits package, including exciting travel perks, generous time\-off, parental leave, a flexible work model (with some pretty cool offices), and career development resources, all to fuel our employees' passion for travel and ensure a rewarding career journey. We’re building a more open world. Join us. Expedia Group B2B is looking for a strategic forward\-looking **Director, Strategy and Integration** to play a meaningful role in evolving our business and redefining the travel industry. Do you want to help people go places? Come travel with us! In this role, you will accelerate the execution of Expedia Group fast growth B2B branch, starting by leading the business integration of acquired companies into our Expedia Group portfolio. Besides this you will be responsible for strategic projects that drive transformational change for our B2B partners across our Lodging, Air and Ground Transport businesses. This includes defining objectives and priorities, evaluating investment priorities and ensuring results. If you have a passion for M\&A, enjoy being results\-oriented, collaborative, and owning end\-to\-end strategic projects then join this dynamic and mighty team! **What you'll do:** ------------------- * Collaborating with key functional leaders, corporate, HR and finance, lead business, product and tech, strategy and commercial integration of acquired company for Expedia Group * Work with third party suppliers for the execution of the integration * Recognize and frame strategic opportunities for Expedia B2B, with a focus on external, in a structured, analytical way to clearly communicate options, risks, and trade\-offs * Drive decision\-making and alignment by working across E4B and Expedia Group * Lead strategic projects and lead investigations to drive the business forward * Travel required, in Amsterdam in year 1 **Who you are:** ---------------- * You have a solid track record of Post Merger Integration and M\&A * You bring excellent quantitative, analytical and critical thinking skills and an ability to translate metrics, research and trends into viable strategies * You have excellent oral and written communication skills to communicate issues and influence others, including experience communicating complex information to senior leaders * You see the 'big picture' and to effectively prioritize and drive multiple projects * You are a self\-starter who can excel in a fast\-paced and fluid environment * You are a team player who actively promotes \& encourages diversity of thought * 10\+ years’ experience in strategy consulting and / or similar role in a leading technology company; MBA a plus * Expert level knowledge of Microsoft Excel and PowerPoint and proven experience in modeling, analysis, research and presentation creation **Accommodation requests** If you need assistance with any part of the application or recruiting process due to a disability, or other physical or mental health conditions, please reach out to our Recruiting Accommodations Team through the Accommodation Request. We are proud to be named as a Best Place to Work on Glassdoor in 2024 and be recognized for award\-winning culture by organizations like Forbes, TIME, Disability:IN, and others. Expedia Group's family of brands includes: Brand Expedia®, Hotels.com®, Expedia® Partner Solutions, Vrbo®, trivago®, Orbitz®, Travelocity®, Hotwire®, Wotif®, ebookers®, CheapTickets®, Expedia Group™ Media Solutions, Expedia Local Expert®, CarRentals.com™, and Expedia Cruises™. © 2024 Expedia, Inc. All rights reserved. Trademarks and logos are the property of their respective owners. CST: 2029030\-50 Employment opportunities and job offers at Expedia Group will always come from Expedia Group’s Talent Acquisition and hiring teams. Never provide sensitive, personal information to someone unless you’re confident who the recipient is. Expedia Group does not extend job offers via email or any other messaging tools to individuals with whom we have not made prior contact. Our email domain is @expediagroup.com. The official website to find and apply for job openings at Expedia Group is careers.expediagroup.com/jobs. Expedia is committed to creating an inclusive work environment with a diverse workforce. All qualified applicants will receive consideration for employment without regard to race, religion, gender, sexual orientation, national origin, disability or age.

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

Negotiable Salary

Indeed

Quality Intern

**Title:** **Quality Intern** ============================= Location: Arganda del Rey, ES *At Tetra Pak we commit to making food safe and available, everywhere; and we protect what's good – protecting food, protecting people, and protecting the planet. By doing so we touch millions of people's lives every day.* *And we need people like you to make it happen.* ***We empower you to reach your potential with opportunities to make an impact to be proud of – for food, people and the planet.*** **Job Summary** --------------- We are looking for an Quality Intern to join Tetra Pak factory based in Spain, Arganda del Rey. This is a paid internship opportunity for a 6\-month \+ 6\-month period. You will be contracted through the Business School or University with a collaboration agreement signed and in force with Tetra Pak Envases S.A. Therefore, a **valid student status** is a must for this position. **What you will do** -------------------- * You will actively collaborate in the implementation and maintenance of the World Class Manufacturing methodology, especially in Quality. * You will be incorporated into the Quality department and will actively collaborate in all functions and tasks aimed at the development of quality methodology: Audits to groups / participation in the weekly strategic meetings of the group, collaboration in the analysis of defects and in the establishment of the conditions for 0 defects. * You will participate in the tasks and projects of the Quality Department, actively collaborating in the management of the quality. * You will gain a deep insight into the WCM (TPM) philosophy of continuous improvement and deep knowledge of one of the main pillars of WCM. **We believe you have** ----------------------- * Active student status at a university or Higher Educational / Business School within the Industrial Engineering / Quality / Manufacturing area * Fluent language skill in English and Spanish * Strong interest and passion to learn more about WCM and Quality methodology * Keen eye for details and highly responsible person **We Offer You** * A variety of exciting challenges with ample opportunities for development and training in a truly global landscape * A culture that pioneers a spirit of innovation where our industry experts drive visible results * An equal opportunity employment experience that values diversity and inclusion * Market competitive compensation and benefits with flexible working arrangements **Apply Now** If you are inspired to be part of our promise to protect what’s good; for food, people, and the planet, apply through our careers page at https://jobs.tetrapak.com/. This job posting expires on **25th December 2025\.** If you have any questions about your application, please contact **Turan Abdullazade at Turan.Abdullazade@tetrapak.com** *Diversity, equity, and inclusion is an everyday part of how we work. We give people a place to belong and support to thrive, an environment where everyone can be comfortable being themselves and has equal opportunities to grow and succeed. We embrace difference, celebrate people for who they are, and for the diversity they bring that helps us better understand and connect with our customers and communities worldwide.*

P.º de la Estación, 28D, 28500 Arganda del Rey, Madrid, Spain

Negotiable Salary

Intern Clinical Operations FSP64706871051394125

Indeed

Intern Clinical Operations FSP

**Work Schedule** Standard (Mon\-Fri)**Environmental Conditions** Office**Job Description** Job Description Are you a student of a Master Degree in Clinical Research who would like to take his\\her first steps within a dynamic clinical research organization? Are you interested in learning fundamental skills to start optimally your career? At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life \- enabling our customers to make the world healthier, cleaner and safer. We provide with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life\-changing therapies. With clinical trials conducted in 100\+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. How will you make an impact? The 6\-month internship in Clinical Operations is designed to offer you the opportunity to develop insight into clinical research, master your skills while conducting meaningful work within the team. The program framework is crafted to allow you to grow professionally, learning invaluable skills to help you kick start your career! What you will do? As part of the Clinical Operations, you will work closely as a team, providing support and ideas for day to day activities. Your engagement and level of dedication will ensure that our project teams will receive the administrative and technical support they need. You will have a mentor who will help you navigate through our organization and processes and receive the best support, which will ensure you are on your way to reaching your goals. You will be introduced to many diverse parts of the company and to other interns across Europe. You will have a wide portfolio of exciting tasks to complete. Plus test your natural curiosity in providing administrative and technical support to the team proactively, educating yourself about the clinical research industry and master your skills to measure your business progress. How will you get here? You are undergoing a Master Degree in Clinical Research Having the ability to handle numerous tasks simultaneously Enjoying working in a team You also have excellent administration and organization skills and the ability to prioritize and time handle various tasks Passionate about common goals Demonstrate a positive demeanor and desire to succeed Exhibits a high degree of flexibility in adapting to a changing business environment English and Spanish proficiency Work Environment: At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both expertly and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award\-winning learning and development program, ensuring you reach your potential. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000\+ colleagues, we share a common set of values \- Integrity, Intensity, Innovation and Involvement \- working together to accelerate research, address sophisticated scientific challenges, drive technological innovation and support patients in need. \#StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

C. de Garganta de los Montes, 2-6, Arganzuela, 28045 Madrid, Spain

Negotiable Salary

Intern Clinical Operations64706871067137126

Indeed

Intern Clinical Operations

**Work Schedule** Standard (Mon\-Fri)**Environmental Conditions** Office**Job Description** Are you a last year university student or recent graduate who would like to take his\\her first steps within a dynamic clinical research organization? Are you interested in learning fundamental skills to start effectively your career? At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life \- enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life\-changing therapies. With clinical trials conducted in 100\+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. **How will you make an impact?** The 6 month internship in Clinical Operations is designed to offer you the opportunity to develop insight into clinical research, master your skills while conducting meaningful work within the team. The programme framework is crafted to allow you to grow professionally, learning invaluable skills to help you kick start your career! **What you will do?** As part of the Clinical Operations, you will work closely as a team, providing support and ideas for day to day activities. Your engagement and level of dedication will ensure that our project teams would receive the administrative and technical support they needs. You will have a mentor who will help you navigate through our organization and processes and receive the best support, which will ensure you are on your way to reaching your goals. Being part of the Clinical Operations team, you will be introduced to many diverse parts of the company and to other interns across Europe. You will have a wide portfolio of exciting tasks to complete. Plus test your natural curiosity in providing administrative and technical support to the team proactively, educating yourself about the clinical research industry and master your skills to measure your business progress. **How will you get here?** * You are last year university student looking for an entry level position * You have the ability to handle numerous tasks simultaneously * You enjoy working in a team * You also have excellent administration and organization skills and the ability to prioritize and time handle various tasks * Results oriented * Demonstrate a positive demeanor and desire to succeed * Exhibits a high degree of flexibility in adapting to a constantly evolving business environment * English and French proficiency **Work Environment:** --------------------- At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award\-winning learning and development programme, ensuring you reach your potential. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000\+ colleagues, we share a common set of values \- Integrity, Intensity, Innovation and Involvement \- working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. \#StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

C. de Garganta de los Montes, 2-6, Arganzuela, 28045 Madrid, Spain

Negotiable Salary

Indeed

Measurement Manager

Agency : Havas Media Group Spain Job Description : The Insights Manager is responsible for delivering strategic insights for local clients based on our proprietary research studies. Mission \& Responsibilities Insights* Develop the Agency group’s research and best in class brand studies at local level * Partner with client teams to address insight needs of local clients with relevant and actionable recommendations from study results * Identify, coordinate, manage and supply all ad hoc research studies * Communicate on your research study and/or present results to clients * Formulate powerful presentations highlighting results to provide strong insights and achievable conclusions * Create ad hoc reports based on client briefs, brand audits New business* Actively contribute to new business pitches, developing solid insights * Foster successful global pitch assignments in coordination with Global Strategy teams Previous Experience \& Industry Background* 8\+ years professional experience in marketing or market research * Media, Brand, Consultancy, Market research Qualifications \& Languages:* Bachelor’s or Master’s degree in Business, Marketing, Economics or Qualitative Analysis * Languages: English (Advanced) Soft skills \& Competencies* Quantitative and qualitative research methodologies * Market research * Market intelligence * Marketing strategy * Qualitative Brand, Consumer, Market analysis * Business acumen * Analytical thinking * Ability to draw meaningful and relevant insights \& conclusions from study results * Storytelling * Communication * Presentation * Detail oriented * Team management * Leadership * Collaborative * Interface with clients and multiple stakeholders Technical Skills* Business Intelligence \& Analytics software (i.e. SAP, Oracle) * Insights solutions (i.e. Meaningful Brand, Content IO, Canopy, Perfect Match) * Planning tools (i.e. Polaris Suite, Connect, Smart Planner) * Office software Contract Type : Permanent Here at Havas across the group we pride ourselves on being committed to offering equal opportunities to all potential employees and have zero tolerance for discrimination. We are an equal opportunity employer and welcome applicants irrespective of age, sex, race, ethnicity, disability and other factors that have no bearing on an individual’s ability to perform their job.

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

Negotiable Salary

Postdoctoral Researcher for the Hereditary Cardiomyopathies Group64695238972034128

Indeed

Postdoctoral Researcher for the Hereditary Cardiomyopathies Group

The Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P.) (CNIC) was established to conduct world-class, competitive, and internationally relevant research on cardiovascular diseases. The CNIC operates a 24,000 m² research center located in Madrid, including over 6,000 m² of state-of-the-art laboratories equipped with cutting-edge infrastructure and technology. **Responsibilities:** * Lead research projects focused on the genetics of Dilated Cardiomyopathy. * Actively participate in the group’s ongoing research lines. * Support the initiation and execution of clinical trials in the field of genetic cardiac diseases. * Participate in preparing and writing results for publication in scientific journals. **Mandatory Requirements:** * Hold a Bachelor’s or Master’s degree in Medicine. * Specialization in Cardiology (MIR). * Hold a Doctorate degree in Life Sciences. * At least two years of postdoctoral research experience in Biomedicine (1 year and 4 months for applicants with a disability exceeding 66%; 1 year and 8 months for applicants with a disability exceeding 33%). **Desirable Requirements:** * C1. Number of first-author publications in cardiovascular genetics will be considered. * C2. Number of publications in which the candidate has participated in the field of cardiac amyloidosis will be considered. * C3. Experience interpreting genetic studies. * C4. Membership in the Working Group of the Spanish Society of Cardiology – Section on Familial Cardiomyopathies and Cardiovascular Genetics. * C5. Membership in the Working Group of the European Society of Cardiology – Myocardium and Pericardium Working Group. * C6. Interview. Positive Action: A correction factor of 1.5 per year of experience will be applied to the calculation of years of experience for evaluation criteria where experience is assessed, in cases where the applicant certifies a disability exceeding 66%; a correction factor of 1.2 will apply if the certified disability exceeds 33%. **Offer:** * Integration into an internationally recognized research center in the scientific domain. * Access to infrastructure equipped with the most advanced technology. * Integration into dynamic, young teams within an environment of scientific excellence. * Immediate incorporation. * A three-year postdoctoral contract, extendable up to a maximum of six years, in accordance with Article 22 of the Law on Science, Technology and Innovation (Consolidated Text of Law 14/2011, of 1 June, on Science, Technology and Innovation), provided the selected candidate meets the legal requirements for formalizing the contract under Spanish labor legislation. **Selection Process:** The “Resolution of the State Secretariat for Public Administration Approving Common Operational Criteria in Selection Processes for Entities of the State Public Sector”, dated 11 April 2022, states in point 6.1 that “Unless specific regulations provide for a competitive examination system, the selection system shall be a combined competition-examination system.” In the case of CNIC, the specific regulation approved by the Foundation’s Board establishes a competitive selection process with an interview phase. A personal interview will be conducted with at least the top three candidates achieving the highest scores, provided their cumulative score across evaluative criteria (C1–C5) reaches at least 60 points. The candidate with the highest overall score (C1–C6) will be hired, provided they achieve at least 75 points. **Evaluation Committee Composition:** * Group Leader * Collaborating Scientist * Coordinator of the Research Office * Manager of the Research Office * HR Representative The CNIC guarantees, within its scope of operations, the principle of equal opportunity in employment access, prohibiting any direct or indirect discrimination based on origin—including racial or ethnic background—sex, age, marital status, religion or beliefs, political opinions, sexual orientation and gender identity, gender expression, sex characteristics, trade union membership, social condition, language within the State, or disability—provided applicants possess the necessary aptitude to perform the required work or job. By participating in the selection process, applicants consent to the inclusion of their personal data in official public resolutions related to the selection process. Such resolutions (provisional list of admitted and excluded candidates; definitive list of admitted and excluded candidates; final resolution of the selection process) will be published on the CNIC website. Scoring Criteria: C1 – Number of first-author publications in cardiovascular genetics – 20% C2 – Number of publications in which the candidate has participated in the field of cardiac amyloidosis – 20% C3 – Experience interpreting genetic studies (evaluated holistically, considering time/specialty relationship) – 20% C4 – Membership in the Working Group of the Spanish Society of Cardiology – Section on Familial Cardiomyopathies and Cardiovascular Genetics (a certificate of active membership must be submitted) – 10% C5 – Membership in the Working Group of the European Society of Cardiology – Myocardium and Pericardium Working Group (a certificate of active membership must be submitted) – 10% C6 – Interview – 20%

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

Negotiable Salary

Indeed

Business Development

**Job Description** The Business Development will be responsible for managing client relationships and internal stakeholders to drive commercial development through a portfolio of advanced consumer panel solutions. This role involves interpreting client briefs, identifying growth opportunities, and designing tailored proposals and research studies. The consultant will oversee projects from start to finish, ensuring timely and high\-quality delivery. Additionally, they will lead the analysis of research results, extract actionable insights, and present findings to clients in a clear, compelling, and strategic manner. **RESPONSIBILITIES** * Own, meet and ‘smash’ the individual revenue target (Forecast and report out of targets and budgets). * Target new clients via different channels and grow the business within the existing client portfolio assigned with our core retail measurement service, prioritize client visits based on sales potential and build a sustainable external network. * Identify upselling opportunities by creating leads for international retail measurement data and the more advanced / customized NIQ services enabling to transform ad\-hoc relationships into continuous partnerships. * Execute end\-to\-end sales process from feasibility analysis; including and pricing, negotiating terms, writing proposals, and closing the sale. * Monitor progress against revenue target with tenacity and course correct quickly where necessary by making maximum use of the available CRM tools * Utilize with creativity the tools available within the wider organization to generate leads and build your internal network * Develop pragmatic engagement plans for the key prospects \& clients in your portfolio * Ensure that all sales materials, including proposals, software\- \& service demos are consistent and demonstrate best in class within the industry. * Initiate \& Drive projects to bring new product /market combination successfully to the market * Work with other NIQ departments to ensure alignment and buy\-in. **WHAT DO WE EXPECT FROM YOU?** Are you a high\-energy self\-starter, curious, passionate about sales, growth, building relationships and new business opportunities? Do you enjoy contributing to the great SMB Team result by having individual impact to make the difference? **Our new team member will have:** * Good understanding of the dynamics of the BE FMCG business * Minimum 3\-5 years of experience, preferably gained in Market Research and or FMCG Trade/Category management * Familiar with the specs and usage of retail tracking business services within the market * Skillful in driving client interest and new business through creative proposal\- and solution creation resulting in high client satisfaction level. * Easy connecting with (potential) clients and ability to build and maintain own network among assigned clients \& prospects * Both short\-term and long\-term results oriented * Excellent communication skills, ability to read other’s styles and adapt behavior accordingly. * Fluent in Spanish and English (based in Madrid or Barcelona) * Portuguese language is a plus **WHAT DO WE OFFER?** Besides an attractive salary \& compensation package, NIQ offers flexible working hours and working from home, helping you to create a work/life balance that fits the best for your personal situation. Moreover, you will experience a dynamic, open, international and solution\-oriented environment. You’ll be trained on\-the\-job to develop your skills and experience. \#LI\-FC \#Hybrid **Additional Information** **Our Benefits** * Flexible working environment * Volunteer time off * LinkedIn Learning * Employee\-Assistance\-Program (EAP) **About NIQ** NIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state\-of\-the\-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100\+ markets, covering more than 90% of the world’s population. For more information, visit NIQ.com Want to keep up with our latest updates? Follow us on: LinkedIn \| Instagram \| Twitter \| Facebook **Our commitment to Diversity, Equity, and Inclusion** At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news\-center/diversity\-inclusion

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

Negotiable Salary

Talent Sourcer (f/m/x)646852801520661210

Indeed

Talent Sourcer (f/m/x)

**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**. **Job Description*** 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. **Qualifications*** 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. **Additional Information*** 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

Negotiable Salary

Laboratory Technician | Clinical Analysis | Madrid646852801681951211

Indeed

Laboratory Technician | Clinical Analysis | Madrid

Would you like to join **Novasalud Global Health**, a leading company in corporate health services, clinical analysis, and healthcare assistance? We are seeking a **Senior Laboratory Technician** to join our team in **Madrid** for **clinical analysis and blood draws** at a **medical center**, for an **approximate period of 6 months**, from **Monday to Friday (working days).** **Main responsibilities:** * Performing clinical analyses, blood draws, and collection of biological samples. * **Pre-analytical procedures** and **sample preparation** for shipment to the laboratory. * **Incident management** and **order management**. **Requirements:** * Qualification as a **Senior Technician in Clinical and Biomedical Laboratory** or equivalent. * Prior experience in **clinical analysis and blood draws**. * Availability of a **personal vehicle** is desirable. **Job conditions:** * Working schedule: **Monday to Friday (working days).** * Working hours: **8:30 a.m. to 10:30 a.m.** * Contract type: **Fixed-term intermittent contract.** * Start date: **Immediate.** * Duration: **Approximately 6 months; possible extension.** * Gross salary: **€500/month** **What we offer:** * Job stability and flexibility. * A dynamic and professional work environment. * Ongoing training in clinical analysis. * Compatibility with another job. **How to apply:** Submit your updated CV by clicking "Apply now" and join our team. **Also...** Join our WhatsApp channel (we post job openings daily) here → https://goo.su/q3nXnLh Job type: Part-time, Fixed-term intermittent contract Contract duration: 6 months Salary: €500.00 per month Work location: On-site

Ronda del Caballero de la Mancha, 68, Fuencarral-El Pardo, 28034 Madrid, Spain

€ 500/week

Integrated Research - Senior Consultant646852800268831212

Indeed

Integrated Research - Senior Consultant

Madrid, Spain \| Full time \| Hybrid \| R1505719**Job available in additional locations** **Location:** Portugal, Spain, Greece**Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence\-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world\-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We’re purpose\-driven problem solvers, that do what we love to make a greater impact on human health.**Integrated Research***We focus on understanding the behaviours and attitudes of Health Care Professionals and patients, and supporting international pharmaceutical companies to understand them as people. This is across the product lifecycle.**We explore and measure what Health Care Professionals and patients say and do using different behavioural frameworks to deliver actionable insights and clear answers to our clients’ business questions. We typically use IQVIA data to contextualise our research and collaborate with other IQVIA teams to provide our clients with comprehensive solutions to their business issues.***The Role** In this role, you’ll be ensuring on\-time and on\-budget delivery of completed projects for high client satisfaction. We need insightful, detail\-oriented people that can identify and elevate new business opportunities and assist in sales, so we can work with our clients to make a difference in the life science industry.**What You’ll Be Doing*** Providing day\-to\-day client management of projects, including leading update meetings, and participating in delivery workshops. Participation in key aspects of project delivery, such as interview moderation, designing, structuring and delivering client reports and presentations * Leading the definition of research design and planning for proposal purposes * Leadership of extended project teams to execute high quality research across multiple methodologies (RWD, PMR, AIML etc) and analysis on time and within budget * Planning, organising and managing all aspects of project delivery (scope, quality, resources, risk and timelines) to successfully complete specific project goals and objectives. Proactively identifying project related delivery risks and suggesting and implementing mitigating actions * Preparing and facilitating decision making on project related questions, internally as well as with clients. Recommending improvements and alternative solutions to resolve client challenges * Identifying new business opportunities for follow\-on work * Supporting business development activities, including proposal writing, pitch development and delivery * Contributing to the EMEA community through networking and cross\-team working * Raising the external profile of IQVIA by attending conferences and generating thought leadership pieces **Who You Are*** A university degree holder with 5\+ years of experience in life science or healthcare consulting * Previous work experience of at least 6/7 years in consultancy and / or market research. Preferential consideration will be given to candidates with experience in carrying out consulting and market research projects in the pharmaceutical area at an international/cross\-country level. * Project management experience with client\-influencing and relationship\-building skills * High skills of interpretation and analysis (quantitative, qualitative and integration of different sources of data assets) * Experienced in developing relationships with senior roles at our client organisations * Knowledgeable of developments in the life science industry * Excellent at presenting and communicating * Fluent in English 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

Negotiable Salary

Pharmaceutical Sr Market Research – French Speaker646852800606751213

Indeed

Pharmaceutical Sr Market Research – French Speaker

Madrid, Spain \| Full time \| Home\-based \| R1479538 We are looking for a passionate a**Pharmaceutical Sr Market Research – French Speaker** to join our dynamic team in Madrid or Barcelona. You will play a key role in managing and delivering primary market research projects, supporting our clients in their strategic decision\-making.**Your responsibilities:*** Lead or contribute to consulting projects from design to delivery. * Analyze client needs and propose tailored, cost\-effective, and innovative solutions. * Supervise and support analysts and consultants throughout project execution. * Conduct qualitative and quantitative analyses to identify key insights. * Produce and present clear, impactful reports adapted to different stakeholders. * Participate in identifying business opportunities and developing client relationships. * Ensure post\-delivery follow\-up to guarantee client satisfaction. * Develop your sector and methodological expertise within our Center of Excellence. **Requirements:*** Ideally, a scientific background and/or graduate from a business school or university. * 5 to 8 years of experience in market research, preferably in a research institute, consulting firm, or within the life sciences industry. * Strong project management and client relationship skills. * Ability to work in teams and manage multiple projects simultaneously. * Excellent verbal and written communication skills, with strong presentation abilities (in French and English). * Good knowledge of consulting methodologies and industry challenges. * Established professional network in the life sciences field is a plus. **Why join us?*** Exciting projects with key industry players. * Collaborative and supportive work environment. * Opportunities for professional growth and specialization. * Flexible hybrid work model. * IQVIA recognized as a LinkedIn Top Employer. * Rich and diverse training offerings. 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

Negotiable Salary

Associate Biostatistics Director - FSP (Permanent Home-based)646852800770581214

Indeed

Associate Biostatistics Director - FSP (Permanent Home-based)

Madrid, Spain \| Full time \| Home\-based \| R1503450**Job available in additional locations** * Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. * Influence and contribute to clinical development plans, collaborate with cross\-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. * Provide statistical thought partnership for innovative study design and clinical development plans, including Go\-No Go criteria and probability of technical success calculations. * Provide for project\-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions. * Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) * Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. * Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge **Education**+ PhD or MS in Biostatistics, Statistics or related field **Experience*** Minimum of 8 years of experience in clinical trial statistics, preferably within a pharmaceutical or CRO setting. *  **Technical Expertise:** * Advanced proficiency in SAS / R for data analysis and statistical programming. * Experience with Bayesian methods, predictive modeling, and simulation techniques. * Proven track record in strategic study design, including adaptive designs, sample size calculations, and interim analysis planning. * Familiarity with regulatory guidance on statistical methodologies (e.g., FDA, EMA, PMDA). * Solid experience in applications of advanced statistical methodologies * Leading roles in regulatory submissions * Experience in interactions with major regulatory authorities preferred * Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full\-) clinical development strategy *  **Study Design and Strategy:** * Ability to lead statistical discussions during protocol development and study planning. * Skilled in defining statistical analysis plans (SAP) and developing strategic approaches for complex study designs. * Experience in strategy discussions involving adaptive design, go/no\-go criteria, and futility analyses. *  **Collaboration and Communication:** * Strong communication skills to effectively present statistical concepts to cross\-functional teams. * Proven experience in collaborating with clinical and regulatory teams to align statistical strategy with overall program objectives. 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

Negotiable Salary

Integrated Research - Senior Principal646852800108811215

Indeed

Integrated Research - Senior Principal

Madrid, Spain \| Full time \| Hybrid \| R1492192**Job available in additional locations** **Location:** EU\-Wide (hybrid/remote)**Real World Commercial Solutions to Create a Healthier World** In RWCS we’re passionate about improving the life sciences ecosystem and making decisions that accelerate innovation for a healthier world. Every day our team develops evidence\-based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We design and deliver Commercial Analytics, supported by our world\-class proprietary data assets, solve complex client challenges through strategic consulting, and use leading edge market research techniques to support clients brand strategy, planning and measurement. We’re purpose\-driven problem solvers, that do what we love to make a greater impact on human health.**Integrated Research***We focus on understanding the behaviours and attitudes of Health Care Professionals and patients, and supporting international pharmaceutical companies to understand them as people. This is across the product lifecycle.**We explore and measure what Health Care Professionals and patients say and do using different behavioural frameworks to deliver actionable insights and clear answers to our clients’ business questions. We typically use IQVIA data to contextualise our research and collaborate with other IQVIA teams to provide our clients with comprehensive solutions to their business issues.***The Role** In this role, you’ll be a senior lead in the Integrated Research team. You will drive the growth of the team across multiple different areas, and be a leadership role model to the other seniors in the group. You’ll work directly with multiple clients to develop business opportunities and provide valuable input to solutions, take pride in your work and relationships, and exceed targets. You will also have a strong focus on developing future talent in the team and ensuring the next generation of leaders has clear guidance and growth pathways**What You’ll Be Doing*** Proactively bringing solutions to ensure the business is well functioning and the teams have what they need to deliver * Owning significantly sized accounts and meeting or exceeding revenue targets by developing and delivering insightful, value\-added solutions that address complex issues * Supporting the evolution of what the team does and how we talk about it to ensure the offering is always compelling to clients * Seeking out and identifying new revenue opportunities and ensuring a continuous flow of business from clients * Applying consultative problem\-solving skills to be an Integrated Solutions expert (based on a foundation of market research) * Developing new, tangible and commercial offerings * Bringing solutions to growth barriers in the business and taking responsibility for their implementation * Contributing to the awareness of IQVIA Integrated Research in the marketplace through speaking engagements, client meetings, and publications * Mentoring, coaching, and sharing expertise **Who You Are*** A degree holder with 15\+ years’ experience in life sciences or healthcare consulting * Expertise in primary market research methodologies and delivery processes * Proven seller of complex engagements to the top Pharma/Life Sciences companies * An established leader, typically of multiple or significantly sized teams, with a record of management and people development * An expert in the identified teams’ solutions, that can produce new and creative ideas * A successful mentor, talent retainer and confident leader that can enable creativity in others **Benefits** Visit our **benefits page** for information on everything from perks to well\-being initiatives and career enhancement. 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

Negotiable Salary

Secondary School Teacher of Biology and Physics-Chemistry646657167262741216

Indeed

Secondary School Teacher of Biology and Physics-Chemistry

We are seeking a qualified secondary school teacher to teach Biology and Physics-Chemistry in ESO and Bachillerato at our school located in Pozuelo. The subject is taught in Spanish. We offer full-time employment and a permanent contract. Start date: End of January Requirements: -Bachelor's degree or equivalent in Biology, Physics, Chemistry, or related fields -CAP or Master's degree in Secondary Education -Availability starting in January Position type: Full-time, Permanent contract Work location: On-site employment

C. Tomás Pierri, 1, 28223 Pozuelo de Alarcón, Madrid, Spain

Negotiable Salary

Study Support Assistant646290684053781217

Indeed

Study Support Assistant

Study Support Assistant 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 As a Study Support Assistant, you’ll play an important role in helping our clinical studies get up and running efficiently. This is an ideal position for someone looking to begin a career in clinical research, offering hands\-on experience in a global organization and the chance to learn from experts in the field. Your main responsibilities will include:* Supporting Study Start\-Up activities by tracking, filing, collating and verifying submission documentation for Ethics Committees (EC), Regulatory Authorities (CA), and other relevant bodies * Assisting with translation and coordination of submission documents * Updating and maintaining tracking systems to ensure accurate study progress records * Assisting in the setup, maintenance, and quality review of the Trial Master File (TMF) to ensure completeness and inspection readiness * Helping set up and maintain electronic filing systems and study documentation * Coordinating and attending team meetings, preparing presentations and materials when required * Assisting with payments to regulatory or ethics bodies as needed * Ensuring compliance with ICH\-GCP, ICON Standard Operating Procedures (SOPs) and study requirements What You Need* A Bachelor diploma (or local equivalent) is required; a background in research or healthcare is an advantage but not essential * Excellent attention to detail and strong organizational skills * Effective written and verbal communication skills in English * A proactive attitude with the ability to collaborate and support multiple team members * Good computer literacy and willingness to learn ICON systems, including CTMS and TMF tools \#LI\-PD1 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

Negotiable Salary

Sr Medical Writer - Narrative Writer646172586382101218

Indeed

Sr Medical Writer - Narrative Writer

**Description** Sr Medical Writer \- Narrative Writer 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 ContributionIndividual 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.

C. del Gral. Cabrera, 29, Tetuán, 28020 Madrid, Spain

Negotiable Salary

Quality Systems Technician646097993662731219

Indeed

Quality Systems Technician

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 full potential. From autonomous vehicles to life-saving robots, our digital technology and software experts think beyond convention, delivering unique R&D and engineering services across all industries. We are seeking a Quality Technician for the Pharmaceutical Sector in Madrid, within our Quality department. What will you do? * Quality Management Systems management. * Administration and tracking of deviations and CAPAs affecting the engineering area. * Technical documentation management and control. * Ensuring compliance with GMP regulations and internal standards. * SAP management. * Basic user-level administration of the SAP Maintenance Module (Plant Maintenance, Quality Management). * User onboarding and offboarding (operators, technicians, etc.), profile and permission assignment. * Reviewing and assigning work orders within the system. What profile are we looking for? * Vocational training (FP) or Engineering degree. * Minimum 3 years’ experience in roles similar to the one offered. * English level B2. * SAP and document management experience is desirable. * Pharmaceutical industry experience is mandatory. Candidates with a disability certificate will be positively considered under our inclusion and diversity policy. We welcome all applications. We offer an extensive training portfolio—including classroom, online, and certification programs. 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 all employees and ensure fair, non-discriminatory selection processes—regardless of ethnicity, nationality, social origin, age, sexual orientation, gender expression, religion, or any other personal, physical, or social circumstance. Why will you enjoy working here? We offer a comprehensive suite of Development and Work-Life Balance measures, including: * A uniquely positive workplace environment, highly rated by our professionals in periodic evaluations. * 24 vacation days + 2 personal days + December 24 and 31 + option to purchase up to 7 additional vacation days per year. * Flexible Compensation Plan (health insurance, transportation, training, meal card or food allowance, childcare support, etc.). * Continuous learning opportunities through MyLearning, Capgemini University, Digital Campuses, and Professional Communities. You’ll also have access to platforms such as Coursera, Udemy, Pluralsight, Harvard Manager Mentor, and Education First for language learning (English, French, German, etc.)—among others! * Life and Accident Insurance. Why Capgemini Engineering? Capgemini is a global leader in partnering with organizations to transform and manage their businesses by harnessing the power of technology. Every day, the Group is guided by its purpose: to unleash human energy through technology for an inclusive and sustainable future. Capgemini is a responsible and diverse organization of over 360,000 team members across more than 50 countries. With a solid 55-year heritage and broad industry expertise, Capgemini is trusted by clients to address their full business needs—from strategy and design to operations—powered by the fast-evolving worlds of cloud, data, AI, connectivity, software, digital engineering, and platforms. In 2022, the Group reported global revenues of €22 billion. Apply now! 'Get the future you want! #LI-AD14 Ref. code 372666-es_ES Posted on 02 Dec 2025 Experience level Experienced Professionals Contract type Permanent Location Madrid Business unit Engineering and R&D Services Brand Capgemini Engineering Professional communities Manufacturing & Operations Engineering

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

Negotiable Salary

Predoctoral researcher in training.645619911038741220

Indeed

Predoctoral researcher in training.

A 4-year predoctoral training contract is offered for the completion of a doctoral thesis at the Center for Metabolomics and Bioanalysis (CEMBIO), Faculty of Pharmacy, San Pablo CEU University, within the framework of the project: ADVANCED DEVELOPMENTS AND STRATEGIES FOR CURRENT CHALLENGES: UNCOVERING HIDDEN INFORMATION IN METABOLOMICS (CHALLENGEMET), whose objective is to improve and consolidate methodologies, expand the amount of information obtained, and enhance the understanding of biological mechanisms underlying health and disease conditions through metabolomics and lipidomics. Job responsibilities:* Conducting research tasks related to the project: Preparation of biological samples and metabolite analysis by mass spectrometry coupled with chromatographic techniques and related methods, data processing and reprocessing using innovative strategies, interpretation and discussion of results. Reading and writing scientific and outreach texts. * Preparation and defense of a doctoral thesis. * Participation in meetings, seminars, and scientific dissemination activities. * Integration into a multidisciplinary and highly competitive team with international recognition. * Collaboration with leading research groups in their respective fields. Educational requirements:* Degree in Chemistry, Pharmacy, Bioinformatics, Biomedicine, or related sciences that qualifies the candidate for doctoral studies. * Not having previously held a predoctoral contract for more than 12 months. * Knowledge of bioinformatics will be valued. * Proficiency in English at C1 level or equivalent is required. Conditions* Type of contract: Predoctoral (Article 21 of Law 14/2011, of June 1, and Royal Decree 103/2019, of March 1). * Start date: The first day of the corresponding month. * Duration: Up to 4 years. * Working hours: Full-time. * Salary: The call establishes in its article 12.4 the minimum remuneration for predoctoral contracts. * Workplace: Center for Metabolomics and Bioanalysis (CEMBIO), Faculty of Pharmacy, San Pablo CEU University. Required documentation* Updated CV. * Academic transcript. * Motivation letter. * Certificate of English proficiency (optional)

Ctra.Majadahonda-Av.Adolfo Suárez, 28660 Boadilla del Monte, Madrid, Spain

Negotiable Salary

Copy of Agro-Food Laboratory Technician645509424788491221

Indeed

Copy of Agro-Food Laboratory Technician

**Job Opportunity: Agro-Food Laboratory Technician – AENOR** Are you passionate about food safety and technical laboratory analysis? Do you want to be part of a team that ensures the quality of products reaching millions of people? At **AENOR**, we are looking for an **Agro-Food Laboratory Technician** to strengthen our team in Madrid, directly contributing to the reliability of our testing and control services. **What will your experience at AENOR be like?** **Reference technical environment** You will work with advanced technology and accredited methodologies in physicochemical and microbiological testing. **Collaborative and specialized team** You will join a multidisciplinary team experienced in food legislation, quality, and safety. **Continuous learning** You will have access to technical training and professional development opportunities in the agri-food sector. **Real impact on food quality** Your work will directly contribute to ensuring the safety of products reaching consumers. **Differentiating benefits** Intensive working hours during summer, flexible compensation, childcare assistance, language training, laptop, meal allowances, and more. **What are we looking for?** * **Technical education**: Higher Vocational Training in Analysis and Control, Clinical Diagnostic Laboratory, Chemistry, or similar. * **Experience**: At least 2 years in an agri-food laboratory performing physicochemical and microbiological tests. * **Regulatory knowledge**: Familiarity with standards such as ISO 17025. * **Rigour and organization**: Ability to follow procedures, record results, and maintain traceability. * **Commitment to quality**: Attention to detail and a vocation for continuous improvement. * **Availability to work shifts and flexible working hours**. **Your mission in the laboratory** You will perform quality control tests on food products, following accredited protocols. You will collaborate in method validation, equipment maintenance, and process improvement. You will actively participate in internal and external audits, ensuring regulatory compliance. **Are you interested?**

C. de Miguel Yuste, 12, San Blas-Canillejas, 28037 Madrid, Spain

Negotiable Salary

Research Engineer Intern (Video/Multimodal LLM)645509424134421222

Indeed

Research Engineer Intern (Video/Multimodal LLM)

***Join Tether and Shape the Future of Digital Finance*** At Tether, we’re not just building products, we’re pioneering a global financial revolution. Our cutting\-edge solutions empower businesses—from exchanges and wallets to payment processors and ATMs—to seamlessly integrate reserve\-backed tokens across blockchains. By harnessing the power of blockchain technology, Tether enables you to store, send, and receive digital tokens instantly, securely, and globally, all at a fraction of the cost. Transparency is the bedrock of everything we do, ensuring trust in every transaction. ***Innovate with Tether*** **Tether Finance:** Our innovative product suite features the world’s most trusted stablecoin, **USDT**, relied upon by hundreds of millions worldwide, alongside pioneering digital asset tokenization services. But that’s just the beginning: **Tether Power:** Driving sustainable growth, our energy solutions optimize excess power for Bitcoin mining using eco\-friendly practices in state\-of\-the\-art, geo\-diverse facilities. **Tether Data:** Fueling breakthroughs in AI and peer\-to\-peer technology, we reduce infrastructure costs and enhance global communications with cutting\-edge solutions like **KEET**, our flagship app that redefines secure and private data sharing. **Tether Education**: Democratizing access to top\-tier digital learning, we empower individuals to thrive in the digital and gig economies, driving global growth and opportunity. **Tether Evolution**: At the intersection of technology and human potential, we are pushing the boundaries of what is possible, crafting a future where innovation and human capabilities merge in powerful, unprecedented ways. ***Why Join Us?*** Our team is a global talent powerhouse, working remotely from every corner of the world. If you’re passionate about making a mark in the fintech space, this is your opportunity to collaborate with some of the brightest minds, pushing boundaries and setting new standards. We’ve grown fast, stayed lean, and secured our place as a leader in the industry. If you have excellent English communication skills and are ready to contribute to the most innovative platform on the planet, Tether is the place for you. **Are you ready to be part of the future?** **About the job** * We are looking for talented individuals to join us for an internship in 2025/2026\. MSc/PhD Internships at Tether aim to provide students with the opportunity to actively contribute to our products and research, and to the organization's future plans and emerging technologies. * In our team, you will have the opportunity to participate in the development of the state\-of\-the\-art (SOTA) foundation models, and will also be responsible for optimizing our distributed model training framework continuously. * PhD internships at Tether provide students with the opportunity to actively contribute to our products and research, and to the organization's future plans and emerging technologies. Our dynamic internship experience blends hands\-on learning, enriching community\-building and development events, and collaboration with industry experts. * Applications will be reviewed on a rolling basis. We encourage you to apply early. Please state your availability clearly in your resume (Start date, End date). **Responsibilities** * Research and develop state\-of\-the\-art LLM and/or video or multimodality models to accelerate open\-source progress in the domains. * Implement the application of large models in our business scenarios, like pre\-training, supervised fine\-tuning, post\-training, inference etc. * Continuously optimize the training framework to better adapt to the training of large models on thousands of multi\-node GPUs. * In this role, you’ll have the opportunity to advance the development of open\-source LLM, vision and/or multimodal foundation models and products. You will have the opportunity to collaborate with broader teams across Tether. * MSc/PhD candidate in computer science or a related technical discipline * Related Research Experience at least one of the following areas: LLM, computer vision, multimodality * Be proficient with PyTorch deep learning framework and libraries * Have excellent analytical and problem\-solving skills, logical thinking skills, communication and collaboration skills * Publications in the top AI conferences (e.g., ACL, NIPS, ICML, ICLR, CVPR, ICCV, ECCV, TPAMI, IJCV, etc.) is a nice to have. **Important information for candidates** Recruitment scams have become increasingly common. To protect yourself, please keep the following in mind when applying for roles: * **Apply only through our official channels.** We do not use third\-party platforms or agencies for recruitment unless clearly stated. All open roles are listed on our official careers page: https://tether.recruitee.com/ * **Verify the recruiter’s identity.** All our recruiters have verified LinkedIn profiles. If you’re unsure, you can confirm their identity by checking their profile or contacting us through our website. * **Be cautious of unusual communication methods.** We do not conduct interviews over WhatsApp, Telegram, or SMS. All communication is done through official company emails and platforms. * **Double\-check email addresses.** All communication from us will come from emails ending in **@**tether.to **or @**tether.io * **We will never request payment or financial details.** If someone asks for personal financial information or payment at any point during the hiring process, it is a scam. Please report it immediately. **When in doubt, feel free to reach out through our official website.**

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

Negotiable Salary

Food Quality Technician with English645509423971871223

Indeed

Food Quality Technician with English

At Cominport Distribución SLU, a multinational specializing in the import and distribution of Japanese food products, we are seeking a food quality technician with English proficiency specialized in the food sector for our Madrid headquarters. Main responsibilities: management of quality procedures related to food products, monitoring ISO 22000 regulations, conducting analyses, supplier control (labeling, etc.). Participation in internal training and dissemination of company regulations regarding handling food products, among others. **Requirements** Bachelor's degree in Food Science and Technology or similar fields. Intermediate/advanced level in English reading and writing. Minimum of 1 year of experience in the quality department of the food industry. Additional training such as related master's degrees will be valued. Intermediate level in **Office** (primarily Excel and Word). **We Offer** Stable full-time employment contract within a positive work environment. Standard working hours: 07.00-08.00 to 16.00-17.00 with a break for lunch. **Area - Position** Quality Department. Position type: Full-time Position type: Full-time, Permanent contract Salary: 18.000,00€-21.000,00€ per year Experience: * Food quality department: 1 year (Required) Language: * English (Required) Job location: On-site

Av. Marconi, 1 - PAE Neisa Sur, Villaverde, 28021 Madrid, Spain

€ 18,000/year

Indeed

CNC MACHINING

Join EDIBON, a leading Spanish company internationally recognized for designing and manufacturing educational and research equipment with over 45 years of experience. Headquartered in Móstoles, Spain, and with a young and dynamic team of more than 120 professionals, EDIBON exports approximately 98% of its products to over 140 countries, offering a broad international perspective and direct contact with clients worldwide. Responsibilities * Operate and program CNC lathes for component production, ensuring precision and quality in each manufactured part. * Read and interpret technical drawings and specifications to set up machines. * Perform preventive and corrective maintenance on CNC equipment to ensure proper operation and minimize downtime. * Program the lathe using the machine's own language and interface. Prepare materials and carry out machining operations. Requirements * Minimum of 2 years' experience as a CNC Turner in the industrial sector. * Advanced knowledge in reading technical drawings and using measuring instruments. * Experience with FANUC-type CNC lathes is desirable. * Experience with other types of machining workshop tools and/or milling machines is a plus. Benefits * Friday afternoons off. * Flexible time-off allowance. * Employee parking. * Fixed salary plus performance-based bonus. * Stable position (permanent contract). Join EDIBON as a CNC TURNER and enjoy a high-quality, committed, and professional environment, working with an innovative team in Móstoles.

C. Julio Cervera, 10, 28935 Móstoles, Madrid, Spain

Negotiable Salary

AI Video & Visual Designer "Proteos Biotech"645338567521291225

Indeed

AI Video & Visual Designer "Proteos Biotech"

**AI Creative Specialist – Visual Storytelling (Proteos Biotech)** **Department:** Global Marketing **Reports to:** Global Marketing Director **Location:** Madrid **Contract type:** Full\-time **Position summary:** At Proteos Biotech, we are seeking a creative professional with solid experience in AI-generated visuals (Midjourney, DALL·E, Leonardo.ai, Runway or others) to transform scientific and medical concepts into impactful visual content aligned with the brand’s defined positioning. You will be responsible for leading AI-based visual creative direction, producing images, renders, key visuals, and moodboards that communicate biotechnology, regeneration, and medical aesthetics in an emotional, aspirational, and rigorous manner. **Main responsibilities:** * Create visual concepts and graphic assets using generative AI (Midjourney, DALL·E, etc.) aligned with the global branding of pbserum. * Design key visuals and moodboards for global line-specific campaigns. * Collaborate with design and medical affairs teams to translate scientific evidence into clear, visually appealing imagery. * Generate product image libraries and emotional storytelling assets for reels, websites, training, and PR. * Develop advanced AI prompts (e.g., Midjourney/ChatGPT) to maximize aesthetic consistency, texture, lighting, and visual tone. * Support the creation of realistic 3D renders of vials and packaging, applying the look \& feel defined in the Brandbook. * Maintain consistency with the global visual tone and brand narrative: visible science, authentic beauty. * Participate in brainstorming sessions with external agencies and contribute disruptive visual solutions. * Develop reusable AI templates for the team (e.g., concepts of “emotional bioremodeling,” skin, enzymes, laboratory, natural beauty). **Requirements:** * Proven experience in art direction or digital design using generative AI (advanced-level experience in Midjourney or similar platforms is mandatory). * Strong knowledge of Adobe Creative Suite, Canva, and AI editing platforms (Runway, Leonardo.ai or similar). * Ability to interpret medical and scientific briefs and translate them into compelling visual storytelling. * Aesthetic sensitivity and mastery of composition, color, lighting, and texture. * Knowledge of the beauty\-tech, aesthetic medicine, or dermocosmetic sectors is a plus. * Professional-level English (reading and writing prompts in English). * Proactive, curious attitude with a focus on visual innovation. **We especially value:** * Experience in global aesthetic or health\-tech campaigns. * Portfolio showcasing AI-generated work (mandatory). * Familiarity with the visual language of pbserum (visible science, elegance, real beauty, natural light). * Ability to work under pressure and manage simultaneous projects. **What we offer:** * Join the leading biotechnology lab in recombinant enzymes. * Integration into a multidisciplinary marketing team (scientific, digital, and creative). * Innovative environment with international projects (LATAM, MENA, Europe, USA). * Ongoing training in AI applied to marketing. * Competitive salary based on experience. Position type: Full-time, Permanent contract Salary: €20\.000,00\-€35\.000,00 per year Benefits: * Christmas basket * Company events * Flexible working hours * Summer reduced working day * Reduced working day on Fridays * Company laptop * Free parking * Private medical insurance * Company phone * Meal vouchers Work location: On-site

C. de Garganta de los Montes, 2-6, Arganzuela, 28045 Madrid, Spain

€ 20,000-35,000/year

Waste Management Technician - Quirónsalud University Hospital Madrid (Pozuelo de Alarcón)645332510624021226

Indeed

Waste Management Technician - Quirónsalud University Hospital Madrid (Pozuelo de Alarcón)

**Quirónsalud** --------------- Quirónsalud is the leading healthcare services provider company in Spain. We have internationally renowned experts in the biomedical field and a large team of healthcare and non-healthcare professionals who work every day to offer the highest quality specialized care in our country. At Quirónsalud, we want to attract the best professional talent to continue offering a differentiated healthcare service distinguished by its quality, high level of specialization, and personalized health care. **Job Description** ---------------------------- **At Quirónsalud, your career has a purpose.** At **Quirónsalud**, we are not only leading the healthcare sector; we are **transforming** it. With state-of-the-art technology and a network of more than **58 hospitals in Spain and over 180 healthcare centers in 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:** Waste Management Technician * **Location:** Quirónsalud University Hospital Madrid - Pozuelo de Alarcón. **Responsibilities:** * Open and close the goods loading dock gate. * Receive various waste collection companies. * Weigh waste materials. * Classify and label waste. * Properly document all waste. * Maintain constant contact with companies to schedule pickup days and times. * Participate in various quality audits by providing requested documentation. * Support the maintenance department when placing orders. **What we offer:** * Temporary contract. * Immediate incorporation. * Full-time contract on split shift (from 08.00 to 17.00 hours)**.** **An environment that enhances your development** * You will have the support of an experienced team that will help you strengthen your skills and advance in your career. * **Continuous training**: we will stimulate your learning and development through our **Quirónsalud University** and our specific **training programs**, enabling your personal and professional growth. **We care about your well-being** * **Access to our health and wellness program**, including initiatives such as: + **Health care:** physical and mental wellness plans (access to medical services, health maintenance programs, and psychological support) + **Financial care:** flexible compensation programs, salary management facilities, and exclusive discounts. + **Family care:** initiatives focused on promoting healthy living and work-life balance. + **Volunteer program.** We are waiting for you! *At Quirónsalud, we promote integration and respect for diversity. Therefore, our selection processes will be conducted under these principles. Likewise, the company declares its commitment to establishing and developing practices that promote and encourage equal treatment and opportunities between men and women, without direct or indirect discrimination based on gender. This principle is part of our Corporate and People policy, in line with Organic Law 3/2007, of March 22, on effective equality between genders.* **Requirements** -------------- **REQUIRED EDUCATION** * Professional certification, CFGM or CFGS in Environmental Control, Waste Management or similar fields. * Proficiency in Office, especially Excel. * Minimum of six months of experience in a similar role. * Availability for immediate incorporation. * Interest in a replacement contract. **Location:** Pozuelo de Alarcón (Spain)**Type of Contract:** Temporary**Working Hours:** Full-time**Sector:** Health**Vacancies:** 1**Discipline:** Others**Work Mode:** On-site

C. Tomás Pierri, 1, 28223 Pozuelo de Alarcón, Madrid, Spain

Negotiable Salary

Indeed

Chemical Engineer

We are looking for a professional with a completed higher degree or bachelor's degree in Chemical Engineering to join a team. Key responsibilities include supervision and management of manufacturing processes, direct interaction and negotiation with suppliers, and specialized technical advisory. Additionally, the candidate will be responsible for inventory management, resource optimization, and organization of personnel in charge of the technical department. The formulation of new products or improvement of existing ones, monitoring of regulations and legal requirements, as well as calculation and control of manufacturing costs, will also be part of the duties. Proven experience in the manufacturing of products such as detergents, soaps, degreasers, air fresheners, alcohols, solvents, or glycols, along with a positive attitude, proactivity, consistency, and strong organizational skills in a similar position for at least two years is highly valued.

Calle del Dr. Benito, 12, 28341 Valdemoro, Madrid, Spain

Negotiable Salary

Researcher (Fluent Turkish)645332510312971228

Indeed

Researcher (Fluent Turkish)

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. **Please submit a copy of your CV in English.** **Tasks and Responsibilities** * 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 Turkish + 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 another European language or Arabic **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

Negotiable Salary

Indeed

CRA II or Senior

CRA I, II or Senior 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

Negotiable Salary