Medical Director - Hematology/Oncology - Remote U.S/Canada

The Medical Director will provide medical oversight for clinical trials, ensuring adherence to company SOPs, client directives, good clinical practice, and regulatory requirements. Responsibilities include attending and presenting at investigator and sponsor meetings, offering medical consultation to clients, investigators, and project teams, and supporting business development. The role also involves providing medical review and analysis for serious adverse events, marketed product ICSRs, periodic safety reports, and other client deliverables such as labeling reconciliation documents, CTD modules, REMS, RMP, and CSRs. This includes monitoring safety variables, discussing medical concerns with principal investigators and clients, managing signal detection activities, scientifically reviewing aggregate reports, contributing to label updates, supporting dossier maintenance and risk management, and medically reviewing adverse event data from various sources.