- Remote, Canada
- Remote
- Senior
- 5+ years
Provide medical oversight for Phase I-IV clinical trials and observational studies, review safety data, support protocol development, and guide regulatory reporting.
Responsibilities
- Provide medical oversight for Phase I-IV clinical trials and observational studies.
- Review participant eligibility, protocol deviations, adverse events, laboratory data, vital signs, and other safety-related clinical data.
- Support protocol development, Investigator's Brochures, Medical Monitoring Plans, Safety Management Plans, and other clinical study documents.
- Respond to investigator and site safety inquiries and provide medical guidance throughout study conduct.
- Participate in Data Monitoring Committees, Safety Review Committees, and cross-functional study team meetings.
Requirements
- Medical degree (MD, DO, or international equivalent)