International Medical Affairs Manager (m/f/d)
Key Responsibilities:
- Served as a scientific authority for the development, analysis, and dissemination of medical and clinical evidence
- Guaranteed adherence to regulatory standards and internal guidelines (SOPs)
- Contributed to global Medical Affairs strategy development and supported product lifecycle activities
- Functioned as a central liaison between R&D, Regulatory Affairs, and international Medical Affairs teams
- Actively supported medical education initiatives, scientific symposia, and external knowledge exchange
- Established and nurtured long-term collaborations with Key Opinion Leaders (KOLs), Healthcare Professionals (HCPs), and study investigators
- Coordinated and supported advisory boards, expert panels, and strategic stakeholder engagement initiatives
- Partnered on clinical development programs and provided support for Investigator‑Initiated Studies (IIS/IIR)
- Delivered high‑quality scientific expertise to cross‑functional teams and internal training programs
- Continuously evaluated scientific publications, competitor activities, and emerging trends in the medical landscape
Qualifications & Expertise:
- Proven experience managing cross‑functional projects within complex, international matrix organizations
- Solid background in Medical Affairs within the biopharmaceutical industry, including launch readiness and lifecycle support
- Strong scientific communication skills and credibility across therapeutic areas e.g. Hematology, and Oncology
- In‑depth understanding of drug development processes, regulatory environments, HTA requirements, and Early Access pathways
- Self‑driven, collaborative professional with a results‑focused mindset and strong commercial awareness
- Demonstrated ability to engage effectively with KOLs, HCPs, and senior internal stakeholders
Requirements:
Start: March 2026
Duration: 10 months
Capacity: 4-5 days per week
Location: remote & onsite (Hybrid 2–3 days/week in office)