Senior Medical Director - Oncology Job at CSG Talent, Cambridge, MA

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  • CSG Talent
  • Cambridge, MA

Job Description

Position: Senior Medical Director - Oncology Clinical Development

We're seeking an accomplished Medical Oncologist or Radiation Oncologist to provide strategic and operational leadership across oncology clinical trials (Phase 0-3). This individual will play a central role in shaping and executing clinical development strategy, working closely with both internal and external collaborators to drive innovative therapies forward.

Overview of Responsibilities:

Clinical Oversight & Execution:

  • Serve as the lead clinical authority for early- and late-stage oncology trials, ensuring robust safety monitoring and data integrity.

  • Provide key medical input on study protocols, development plans, and regulatory submissions.

  • Act as the primary reviewer for safety data and clinical trial deliverables, including investigator brochures, study reports, and annual updates.

  • Partner cross-functionally with regulatory, clinical operations, data management, pharmacology, and medical writing teams to guide trial execution from startup to closeout.

  • Collaborate with imaging experts and scientific teams on exploratory and Phase 0 initiatives.

Strategic Input & Cross-Functional Leadership:

  • Lead cross-functional study teams, driving alignment across clinical and operational stakeholders.

  • Provide medical input on external collaboration opportunities, including investigator-initiated studies, partnerships, and licensing assessments.

  • Support regulatory interactions by contributing to briefing documents and participating in agency meetings as needed.

  • Interface with discovery and business development teams to evaluate new assets or indications from a clinical feasibility perspective.

Qualifications:

  • Medical degree (MD or equivalent) with board certification in oncology or radiation oncology.

  • At least 4 years of clinical research experience in oncology, within an academic, biotech, or pharmaceutical setting.

  • Demonstrated ability to provide medical oversight across the full clinical trial lifecycle.

  • Experience with radioligand therapies (RLT) is a plus but not essential.

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