Medical Monitoring Manager - Oncology
$150,000–$200,000 year
Remote · United States or Raleigh, North Carolina, United States
Job Summary
Lead the Medical Monitoring Unit for oncology trials (Phase I–III); oversee multiple Medical Monitors; provide expert medical guidance on protocol interpretation, safety events, eligibility, and benefit–risk; act as senior medical point of contact for sponsors and investigators; drive consistency, quality standards, and best practices across studies and across the team; manage resource allocation and priorities across a complex and evolving study portfolio; support hiring, coaching, and retention of high-performing medical staff; collaborate with Clinical Operations, Drug Safety, Medical Writing, and Regulatory; 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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