MD/DO - Assoc Medical Mgr PSS / PV REMOTE based in CANADA

Fortrea is currently seeking an Associate Medical Manager - MD / DO (Patient Safety Solutions), to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. This is a full-time, home-based position in Canada. ## What You Will Do You will provide medical safety expertise, directly and indirectly, to sponsor drugs, devices, and combination products in the post marketing world. Other key responsibilities: - Undertake primary medical review of cases, including medical assessment of the case for seriousness, listed/labeling, causality, adverse event coding and narrative review. - Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. - Assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs. - Provide training and guidance to the case processing team on medical aspects of case processing. - Performs secondary medical review (QC role) and retrospective review of cases reviewed (QA role), as required for measuring quality of deliverables, identifying error trends, training needs and areas of improvement. - Undertake any other duties as required YOU NEED TO BRING… - MD or DO with at least 4 years of pharmacovigilance experience (clinical trial and post approval experience) - Comprehensive understanding of US healthcare system - Fortrea may consider relevant and equivalent experience in lieu of educational requirements. - Language skills: English proficient in speaking, writing, and reading. - Working knowledge of medical sciences, diagnosis and therapeutics including drug treatments and procedures. - Knowledge and understanding of regulatory requirements for Clinical Research. - Knowledge and understanding of ICH-GCP guidelines. PREFERRED NEED TO BRING: - MD who has completed an accredited residency program or equivalent and is board-eligible or certified with at least 4 years of experience with substantial knowledge of drug safety and the global regulations governing pharmacovigilance and risk management. - Strong understanding of regulatory requirements relating to Pharmacovigilance. - At least 4 years pharmaceutical industry experience, including and specific to pharmacovigilance (post approval experience, case processing, medical review) and/or clinical research. - 1 to 2 years of clinical practice experience. Position is based remote in Canada This position is not eligible for sponsorship. Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable. The application deadline is Aug 2, 2026 Learn more about our EEO & Accommodations request here.

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