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 workplace. 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.
- 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.
- Perform 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

- 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:

- Medical
- Dental
- Vision
- Life
- STD/LTD
- 401(K)
- ESPP
- Paid time off (PTO) or Flexible time off (FTO)
- Company bonus where applicable

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.

Application deadline is Aug 2, 2026.

EEO & Accommodations request.

At Fortrea, we're all about turning the "impossible" into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

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📌 MD/DO - Assoc Medical Mgr PSS / PV REMOTE based in CANADA (Calgary)
🏢 FTCAN Fortrea Canada
📍 Calgary