Physician

ABOUT BIOPHARMA SERVICES BioPharma Services Inc. is a Toronto-based clinical research organization specializing in Phase 1, first-in-human and bioequivalence studies. We operate a fully equipped clinical trial unit with in-house dosing, continuous telemetry and on-site laboratory capability, supporting sponsors across North America, Europe and Asia. BioPharma Services is a subsidiary of WELL Health Technologies Corp. (TSX: WELL). THE OPPORTUNITY We are seeking a Physician to join our medical team on a part-time employed basis, working on site at our Toronto clinical unit. Reporting to the Chief Medical Officer, you will provide direct medical oversight of study participants across an active portfolio of early-phase protocols. This is a salaried employed position. There is no billing, no overhead, no patient roster and no after-hours call. KEY RESPONSIBILITIES • Conduct screening histories and physical examinations, and determine participant eligibility against protocol criteria • Provide medical coverage during dosing and confinement periods, including real-time assessment and management of adverse events • Review ECGs, laboratory results and vital signs, and act on clinically significant findings • Assess seriousness, severity, causality and expectedness of adverse events, and support safety reporting • Evaluate protocol deviations and contribute to their documentation and resolution • Perform sub-investigator duties in accordance with ICH-GCP, Health Canada Division 5 and the applicable protocol • Support the Principal Investigator with medical review of study data and clinical study reports QUALIFICATIONS Required: • MD or equivalent, with a certificate of registration authorizing independent practice from the College of Physicians and Surgeons of Ontario (CPSO) • Current ACLS certification, or willingness to obtain it before start date • Strong ECG interpretation skills and comfort managing acute clinical events • Sound, defensible clinical judgment and clear documentation practices • Professional liability protection (CMPA) in good standing Considered an asset: • Previous experience as an investigator or sub-investigator in clinical trials • ICH-GCP certification • Emergency medicine, internal medicine or critical care background Prior clinical research experience is not required. We provide full GCP, protocol and investigator qualification training, along with structured onboarding within the medical team. WHAT WE OFFER • Employed part-time position with competitive salary and benefits • Predictable weekday schedule agreed in advance • Exposure to first-in-human drug development across a broad range of therapeutic areas and molecule types • A collaborative medical team and an experienced clinical operations, quality and data management group • Career pathway toward investigator qualification and expanded medical responsibility BioPharma Services Inc. is an equal opportunity employer. We welcome applications from all qualified candidates and provide accommodation throughout the recruitment process on request.

Provide direct medical oversight of study participants in early-phase clinical protocols, including screening and physical examinations. Manage adverse events, review clinical data such as ECGs and lab results, and support the Principal Investigator with medical reviews.

Requires an MD with a valid CPSO registration and current or obtainable ACLS certification. Candidates must possess strong ECG interpretation skills and professional liability protection (CMPA).

• Competitive Salary • Benefits

Identified from the job description. Confirm important requirements above.

• Medical Oversight
• Physical Examinations
• ECG Interpretation
• Adverse Event Management
• Clinical Trial Conduct
• ICH-GCP
• Patient Eligibility Screening
• Safety Reporting
• Clinical Documentation
• Acute Clinical Event Management

• Healthcare
• Science & Research

Minimum education

Master’s degree

Minimum experience

2+ years

Apply by

Sep 8, 2026

Posting language

English

Working hours

40 hours per week

Seniority

Mid-Senior level

Application method

Direct apply is available