SVP Late Clinical Development

Added
30 minutes ago
Type
Full time
Salary
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Related skills

leadership regulatory affairs clinical trials oncology medical affairs

๐Ÿ“‹ Description

  • Provide medical direction for late-stage programs and data-driven decisions.
  • Lead late clinical development function, directly and through reports.
  • Design and execute registrational trials in solid tumors.
  • Serve as Medical lead on clinical programs and represent development teams.
  • Develop clinical strategy, protocols, and regulatory milestones; liaise with KOLs.
  • Maintain data-driven decision making and rigorous data review.

๐ŸŽฏ Requirements

  • MD or equivalent with Oncology/Hematology board certification or eligibility.
  • 12+ years oncology clinical trial and drug development experience.
  • Experience leading medical affairs and global clinical development programs.
  • Strong regulatory filing experience and health authority interactions.
  • Excellent communication and leadership in matrix teams.
  • Deep knowledge of trial methodology and regulatory compliance.

๐ŸŽ Benefits

  • Paid time off, holidays, and sick leave.
  • Medical, dental, and vision plans.
  • Disability and life/AD&D coverage.
  • FSA/HSA options and commuter benefits.
  • 401(k) with ER contributions; Employee Stock Purchase Plan.
  • Pet insurance and employee assistance program.
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