Medical Affairs

Description

Job Summary: We are seeking a Medical Affairs professional to contribute to the scientific and clinical development of health research projects, ensuring methodological rigor and regulatory compliance. Key Highlights: 1. Key role in scientific, clinical, and regulatory support for research. 2. Collaboration with multidisciplinary teams and healthcare professionals. 3. A close-knit professional environment with impact on transforming lives. Seville \| On-site \| 40 hours/week \| Immediate Start At **Duponte**, we believe science holds the real power to transform lives. Our work integrates biomedical research, technology, and purpose to develop innovative solutions in healthcare. In this new growth phase, we seek to hire a **Medical Affairs** professional to contribute to the scientific and clinical development of our research projects, ensuring methodological rigor, regulatory compliance, and high-quality scientific communication. This position will play a key role in providing scientific, clinical, and regulatory support for the company’s research initiatives, collaborating closely with multidisciplinary teams and healthcare professionals. **Your Mission** Provide scientific and clinical support to Duponte’s research projects, ensuring proper review of scientific and regulatory documentation, adherence to protocols and applicable regulations, and accurate interpretation and communication of scientific evidence. You will help ensure that medical and clinical research activities are conducted in accordance with ethical, scientific, and quality principles aligned with international best practices. **Your Responsibilities** Scientific and Clinical Support * Establish and maintain scientific interactions with healthcare professionals and researchers. * Collaborate with internal multidisciplinary teams in developing medical and scientific activities. * Provide scientific and clinical support to research projects. * Review and collaborate in preparing scientific and regulatory documentation, ensuring compliance with protocols and regulations. * Analyze and interpret clinical and scientific data for accurate communication within project contexts. * Prepare and adapt scientific materials for diverse audiences, maintaining methodological rigor and clarity. Regulatory Compliance and Quality * Verify compliance with protocols, Good Clinical Practice (GCP), and ICH guidelines. * Support preparation and review of medical and regulatory documentation. * Ensure traceability and quality of clinical information. Integrated Management System * Participate in internal and external audits as required. * Support development and updating of procedures and system documentation. * Report non-conformities and opportunities for improvement. **What We Require (Mandatory)** Academic Qualifications * University degree in **Health Sciences** (Biology, Medicine, Pharmacy, Biotechnology, Biomedicine, or related disciplines). * **Master’s or postgraduate degree** in Clinical Research, Biomedicine, or related fields. Experience * **More than 2 years of experience** in Medical Affairs, clinical development, or translational research. **What We Highly Value** * Ability to communicate scientific information clearly and rigorously. * Knowledge of Good Clinical Practice (GCP) and ICH guidelines. * Experience in analysis and interpretation of clinical or scientific data. * Experience in reviewing scientific and regulatory documentation. * Experience working with multidisciplinary teams. * Ability to manage multiple projects simultaneously. **What We Offer** * Permanent contract and 40 hours/week. * Immediate start. * A close-knit professional environment with impact. **Selection Process** The full process typically lasts **5 to 6 weeks**. **Commitment to Diversity** In compliance with current equal opportunity legislation, we guarantee equal opportunities throughout selection processes, without discrimination based on gender, age, race, origin, religion, sexual orientation, gender identity, disability, or any other personal or social condition. **Data Protection** By submitting your application, you authorize **DUPONTE INVESTIGACIÓN Y DESARROLLO, S.L.** to retain your personal data and CV for a period of **12 months** for potential future selection processes, even those different from the position to which you are applying. You may exercise your rights at any time by writing to: **protecciondedatos@dupontegroup.com**. Benefits: * Intensive workday on Fridays * Company-provided laptop * Optional remote work Relocation/Moving Possibility: * Seville, Seville province: Commute to work without difficulty or plan relocation before starting work (Mandatory) Experience: * medical affairs: 2 years (Mandatory) Work Location: On-site employment