Associate Director, Publications | Pharmacist (m/w/d)
BioNTech SE
Job Summary
As an Associate Director, Publications, you will be instrumental in developing key scientific publications for BioNTech's oncology portfolio. Your daily responsibilities will include strategic and tactical planning, implementing publication plans, and providing scientific writing support. You will collaborate with internal medical and translational teams, writing teams, and external service providers to produce high-quality publications such as original articles, presentations, posters, and abstracts. This role requires a proven ability to drive medical and scientific publications within a multidisciplinary team, exceptional writing and communication skills, and the capacity to articulate complex scientific concepts clearly and concisely. The position is attractive for professionals with a strong background in medical communications within the biotech or pharmaceutical industry, offering the chance to contribute significantly to cutting-edge oncology research.
Required Skills
Education
Advanced degree in a related scientific discipline or medical degree (e.g., PharmD, PhD, MD)
Experience
- 3+ years of medical communications experience in a biotech, pharmaceutical, or medical communications company as a publication manager/writer
- Proven experience with a global publications database management system (ideally)
Languages
Additional
- Certified Medical Publication Professional (CMPP) certification (advantageous or intent to pursue)
More Jobs from BioNTech SE
Associate Director Data Analytics Platform Architecture | Computer Scientist (m/w/d)
Jul 17, 2025
This Associate Director role focuses on leading architectural decisions for data analytics platforms...
Genomics Core Facility Operator | BTA (m/w/d)
Jul 17, 2025
This role involves hands-on molecular biological work within an operational shift system, adhering s...
Director Global Regulatory Affairs | Pharmacist (m/w/d)
Jul 16, 2025
As the Director Global Regulatory Affairs, you will serve as the Global Regulatory Lead for assigned...