The Medical Director will play a key role in drug safety and pharmacovigilance, serving as a product safety lead for clinical development programs and post-marketing products. This individual will provide medical assessments and interpretation of safety data from multiple sources, including clinical trials, post-marketing reports, aggregate analyses, and literature reviews.

Reporting to the Senior Medical Director of Drug Safety and Pharmacovigilance, this role involves close collaboration with cross-functional teams to support clinical development, regulatory filings, and global post-marketing safety activities. The MD will also assist with pharmacovigilance operations, oversight of safety system vendors, and ensuring compliance with drug safety regulations, risk management practices, and pharmacovigilance standards.