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Senior International Medical Affairs Associate (M/F/D)
Tasks:
Scientific expert for generation, interpretation, and communication of medical data
Ensured compliance with regulatory requirements and internal SOPs
Supported international Medical Affairs strategy and Life Cycle Management (LCM) initiatives
Acted as key interface between R&D, Regulatory Affairs, and International Medical teams
Contributed to medical education activities, symposia, and scientific exchange initiatives
Built and maintained relationships with KOLs, HCPs, and principal investigators
Supported advisory boards, expert meetings, and stakeholder engagement projects
Collaborated on clinical programs and Investigator-Initiated Research (IIR) support
Delivered scientific input for cross-functional teams and training initiatives
Monitored scientific literature, competitive landscape, and emerging medical trends
Qualification:
Cross-functional project management in complex matrix environments
Medical Affairs expertise in biopharma, including product launches and lifecycle management
Scientific credibility and communication across Allergology, Hematology, and Oncology
Knowledge of drug development, regulatory frameworks, HTA, and Early Access Programs
Collaborative, self-directed, and results-oriented with strong business acumen
Stakeholder engagement with KOLs, HCPs, and senior leadership
Operational excellence in planning, prioritization, and execution
Awareness of local regulations, market access, and commercial considerations
Requirements:
Start: March 2026
Duration: 10 months
Capacity: 4-5 days per week
Location: remote & onsite (Hybrid 2–3 days/week in office)
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