Medical Monitoring Manager - Oncology
$111,000–$148,000 year
Hybrid · Toronto, Ontario, Canada
Job Summary
Lead the Medical Monitoring Unit for oncology trials across Phase I–III, providing medical leadership, oversight of multiple Medical Monitors, and ensuring high-quality monitoring across studies. Serve as a senior medical point of contact for sponsors, investigators, and internal stakeholders; drive consistency, quality standards, and best practices; manage resources and study-portfolio priorities; contribute to study/portfolio planning with budgets; support hiring, coaching, and retention of medical staff; collaborate with Clinical Operations, Drug Safety, Medical Writing, and Regulatory. Requires MD with oncology focus and 8–10+ years in clinical research, with proven Medical Monitor experience in oncology trials; strong safety review and medical decision-making background; CRO or pharma experience and cross-functional leadership. Offers flexible working hours with a remote or hybrid model depending on location, and a compensation range of CAD 150k–200k (converted to USD as applicable). English fluency required; Spanish a plus.
Required Qualifications
- Medical Doctor (MD) required; oncology specialization strongly preferred
- 8 –10+ years of experience in clinical research
- Proven experience as a Medical Monitor in oncology clinical trials (Phase I–III)
- Strong background in safety review and medical decision-making in active oncology studies
- Demonstrated experience in people management and team leadership
- Experience managing multiple studies or programs simultaneously
- Strong understanding of clinical trial design and regulatory frameworks (ICH-GCP, FDA, EMA)
- Fluent English required; Spanish is a plus
- CRO experience strongly preferred; Pharma experience will also be considered
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.