Medical Director

• Serve as the primary medical point of contact for investigators, regulatory agencies, and internal/external teams
• Ensure consistent protocol interpretation and address medical inquiries
• Monitor clinical trials and Expanded Access Programs for participant safety, data accuracy, protocol compliance, and timely resolution of medical issues
• Participate in investigator discussions during site selection
• Lead investigator calls to review inclusion/exclusion criteria and support site selection and patient recruitment
• Act as the primary medical expert for the protocol and ensure adherence across stakeholders
• Review and ensure proper documentation and timely reporting of AEs, SAEs, and other safety events
• Provide causality assessments for adverse events, including those requiring expedited regulatory reporting
• Work with DSMBs and safety committees to provide safety oversight and evaluate ongoing trial data
• Deliver training and support to investigators, site staff, and internal/external teams
• Participate in investigator meetings, site initiation visits, and study training
• Lead development of protocols, treatment guidelines, and project documents with medical input on design, endpoints, criteria, and methodology
• Oversee protocol adherence and manage deviations
• Collaborate with clinical operations, regulatory, project management, and pharmacovigilance teams
• Support safety reporting and represent Medical Affairs in bid proposals, bid defences, client presentations, and cross-functional scientific discussions

Explore Medical Director at WEP Clinical. Review requirements and application details.