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Medical Affairs & Safety

Senior Director, Medical Affairs

Lead medical affairs for a targeted radioligand therapy ahead of launch. You will build the field team, the evidence plan and the company's relationships with the nuclear medicine community.

HybridPermanentDirector

A typical mandate

The company develops radioligand therapies that deliver a therapeutic isotope directly to tumor cells. Its lead program is in a Phase 3 study in neuroendocrine tumors, with a companion imaging agent in development. Launch depends on treatment sites being ready, and medical affairs leads that work.

What the role owns

  • Build the medical affairs plan for launch, including scientific communication and education
  • Hire and lead a field medical team covering nuclear medicine and oncology
  • Develop relationships with nuclear medicine physicians, radiation safety officers and oncologists
  • Lead the integrated evidence plan, including real-world and investigator-initiated studies
  • Support site readiness on dosimetry, radioactive material handling and patient pathways
  • Partner with commercial and regulatory on compliant scientific exchange

What great candidates bring

  • MD, PharmD or PhD with 10+ years in medical affairs
  • Oncology medical affairs experience, with radiopharmaceutical or nuclear medicine exposure strongly preferred
  • Pre-launch and launch experience
  • Experience building and leading field medical teams
  • Fluency with the PhRMA Code and OPDP expectations for scientific exchange
  • Comfort working with sites where radiology, oncology and radiation safety meet

Why it matters

  • Reports to the Chief Medical Officer
  • Equity at a company approaching its first approval
  • A defining role in how treatment sites adopt this therapy
  • Hybrid schedule, with regular site travel
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