Medical Scientific Affairs Manager | Referent (m/w/d) Med- Wiss. Arzneimittel
URSAPHARM Arzneimittel GmbH
Job Summary
As a Medical Scientific Affairs Manager in Saarbrücken, you will play a pivotal role in the scientific lifecycle of pharmaceutical products. Your daily responsibilities include planning, coordinating, and providing scientific oversight for preclinical and clinical studies, ensuring all documentation meets rigorous regulatory standards. You will act as a key scientific liaison, creating and reviewing regulatory documents, expert reports, and medical statements for both national and international approval processes. Beyond administrative tasks, you will drive innovation by researching current clinical data to support new product development and answering complex medical inquiries from patients, physicians, and pharmacies. This position is ideal for those who enjoy interdisciplinary collaboration across regulatory, quality, and marketing departments. The role offers a secure, long-term career path within a modern family-owned pharmaceutical company, characterized by a strong welcome culture and competitive compensation under the chemical industry collective agreement.
Required Skills
Education
University degree in Natural Sciences, Pharmacy, Life Sciences, or a comparable field of study.
Experience
- Professional experience in Medical Scientific Affairs, drug regulatory affairs, or clinical research is preferred
- Experience in planning, coordinating, and scientifically monitoring clinical studies
- Proven experience in creating and reviewing regulatory documents and scientific reports
- Experience in interdisciplinary collaboration with quality, marketing, and R&D departments
- Experience in conducting structured scientific literature research and data evaluation
Languages
Additional
- A copy of a valid identity document must be included with the application for identity verification purposes. Applications must be submitted digitally.