Regional Medical Affairs Manager

Role Summary Support regional and overseas medical affairs, including evidence generation, KOL engagement, scientific communication, and cross-functional teamwork. Responsibilities: Lead clinical or epidemiological research: generate protocols, coordinate with investigators, manage operations, and ensure timely study progress. Support manuscript development and publication: discuss results with PIs, review drafts, and drive timely submission. Gather regional regulatory requirements for drugs, engage KOLs, and compile PI lists/site references for global studies. Conduct educational activities (forums, advisory boards, expert meetings) aligned with medical strategy. Support Marketing-led medical education: review slides and provide scientific/clinical data. Map and engage KOLs, maintain expert database, gather insights on unmet needs, and input into R&D and post-launch planning. Help develop medical strategies for innovative products: country-specific evidence/data dissemination plans, annual strategy, and clinical guideline updates. Build and maintain product data sets (slides, literature) and regularly update materials with new evidence. Provide scientific/medical training to international business team and support R&D, Sales, Marketing as needed. Requirements : Master’s/Bachelor’s in Clinical Medicine, Life Sciences, or related disciplines. 6–10 years in medical / clinical affairs, oncology / immunology / infectious disease preferred. Post-market medical activities or cross-border medical affairs experience a plus. Strong communication skills. Comfortable with global/regional teams. Open to business travel internationally. License no. 21C0661 Reg No. R1331018