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San Francisco, CA or Boston, MA
  • Lead overall clinical development strategy across the portfolio, including first-in-human through later-stage studies.
  • Provide medical leadership for protocol design, dose escalation strategy, safety review, and clinical data interpretation.
  • Serve as strategic lead for interactions with FDA, EMA, and other health authorities, including regulatory submissions and development planning.
  • Oversee and help build clinical development, clinical science, and medical affairs capabilities.
  • Partner closely with translational, regulatory, biometrics, and executive leadership to shape development strategy and portfolio decisions.
  • Drive KOL engagement, advisory boards, investigator relationships, and scientific communication strategy.
  • Support safety oversight, benefit-risk assessment, and data-driven go/no-go decisions.
    Contribute to Board presentations, investor diligence, and broader corporate strategy.
  • MD required; board certification in Medical Oncology, Hematology, Hematology/Oncology, or another relevant specialty strongly preferred.
  • 15+ years of biopharma clinical development experience, including senior medical leadership roles.
  • Demonstrated experience advancing oncology or hematology programs through IND, Phase I/II development, and proof-of-concept milestones.
  • Experience serving as medical lead for early phase dose escalation studies, including exposure-response, safety review, and development strategy.
  • Prior experience with solid tumors, hematologic malignancies, cell therapy, radiopharmaceuticals, ADCs, or immuno-oncology
  • Track record of regulatory interactions with FDA and other global agencies.
    Experience in early-stage or venture-backed biotech environments preferred.
Accepted file types: doc, docx, pdf, odt, Max. file size: 100 MB.