Medical Information Manager in Medical Science | Medical Information Manager (m/w/d) im Bereich MedWiss
URSAPHARM Arzneimittel GmbH
Job Summary
As a Medical Information Manager in the Medical Science department, you will play a pivotal role in bridging the gap between scientific data and commercial application. Your day-to-day responsibilities include creating and quality-assuring high-quality training materials for marketing and sales, managing Key Opinion Leader (KOL) relationships both nationally and internationally, and planning medical education formats such as Advisory Boards and CME events. You will be responsible for the scientific positioning of the product portfolio and ensuring all medical communications adhere to internal and external compliance standards. This role is ideal for a professional who enjoys scientific analysis and public representation at congresses. The position offers a secure career in the growing pharmaceutical industry within a modern family-owned company, featuring an attractive salary based on the chemical industry collective agreement and a strong welcome culture in Saarbrücken.
Required Skills
Education
Completed university degree in Medicine, Human Biology, or a related scientific field.
Experience
- Several years of professional experience in Medical Affairs, Medical Information, or as a Medical Science Liaison (MSL)
- Extensive experience in handling medical-scientific studies, statistics, and medical evidence
- Proven experience in scientific analysis and communication with professional circles
- Experience as an Information Officer (Informationsbeauftragter) is highly desirable
Languages
Additional
- Willingness to undertake occasional business travel for congresses and meetings; valid identity document required for the application process; location based in Saarbrücken.
More Jobs from URSAPHARM Arzneimittel GmbH
GMP Documentation Specialist | GMP Documentation Specialist (m/w/d) GMP-Compliance
May 7, 2026
As a GMP Documentation Specialist, you will play a vital role in managing the document lifecycle for...
Deputy Head of Manufacturing (Solid Dosage Forms) | Stellv. Herstellungsleitung (m/w/d) Feste Formen
May 7, 2026
As the Deputy Head of Manufacturing for Solid Dosage Forms, you will play a pivotal role in ensuring...
Technical Specialist, Qualification and Validation (GMP Compliance) | Technischer Mitarbeiter (m/w/d) Qualifizierung und Validierung, GMP-Compliance
May 7, 2026
As a Technical Specialist in Qualification and Validation, you will play a vital role in ensuring th...