The opportunity
The Medical Advisor will lead post-marketing clinical research and real-world evidence (RWE) initiatives to optimize product lifecycle management. This role requires integrating scientific expertise with strategic insights to generate robust evidence supporting product safety, efficacy, and value in real-world settings. The candidate will collaborate cross-functionally to drive data-driven decision-making and ensure alignment with regulatory and market needs.
How you’ll spend your day
Post-Marketing Clinical Research & RWE Strategy
Design and execute post-marketing studies (Phase IV), including protocol development, data analysis, and interpretation of results to address clinical gaps and regulatory requirements.
Lead real-world evidence projects (e.g., observational studies, database analyses) to evaluate treatment patterns, comparative effectiveness, and long-term outcomes.
Collaborate with biostatistics and data science teams to apply advanced analytics (e.g., R, SAS) for RWE generation.
Cross-Functional Collaboration
Partner with Market Access to develop value propositions using RWE for reimbursement and health technology assessments (HTA).
Support R&D activities as needed.
KOL Engagement & Scientific Communication
Build and maintain relationships with Key Opinion Leaders (KOLs), facilitating advisory boards and expert panels to gather clinical insights and drive research priorities.
Compliance & Risk Management
Ensure adherence to GCP, regulatory guidelines (e.g., FDA, NMPA), and internal SOPs in all research activities.
Monitor and assess safety signals from post-marketing data, collaborating with Pharmacovigilance for risk mitigation.
