Medical Monitoring Manager - Oncology
$150,000–$200,000 year
Hybrid · Nashville, Tennessee, United States
Job Summary
Lead the Medical Monitoring Unit for oncology trials (Phase I–III), overseeing multiple Medical Monitors and ensuring high-quality medical monitoring and safety reviews across studies. Provide expert medical guidance on protocol interpretation, safety events, eligibility, and benefit-risk assessments; serve as a senior medical contact for sponsors, investigators, and internal stakeholders; drive consistency and quality standards across the portfolio; manage resource allocation and prioritize competing demands; contribute to study and portfolio planning with budgets and cross-functional collaboration; support hiring, coaching, and retention of medical staff; collaborate with Clinical Operations, Drug Safety, Medical Writing, and Regulatory. This role combines medical depth, leadership responsibility, and strategic influence within a globally focused oncology-oriented organization, with a remote or hybrid work model depending on location and preference.
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
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