Senior Medical Director, Oncology Early Development

Added
20 days ago
Type
Full time
Salary
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Related skills

gcp clinical trials pharmacovigilance clinical study reports regulatory compliance
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📋 Description

  • Oversees direction, planning, execution, and interpretation of clinical trials in one or more
  • Participates in cross-functional teams to deliver high-quality clinical data aligned with product
  • Manages design and implementation of clinical development programs withinProduct Development Plan.
  • Oversees study integrity, enrollment timelines, and safety/efficacy data interpretation.
  • Ensures adherence to regulatory requirements and Good Clinical Practices (GCP).
  • Provides clinical expertise and collaborates with internal stakeholders across functions.

🎯 Requirements

  • Medical Doctor (M.D.), D.O., or non-US MD-equivalent; residency preferred; subspecialty fellowship
  • At least 2 years of clinical trial experience in pharma, academia, or equivalent.
  • Ability to run a clinical research program of moderate complexity with minimal supervision.
  • Strong cross-functional collaboration and communication skills (English).
  • Knowledge of regulatory/compliance requirements and clinical strategy development.

🎁 Benefits

  • Competitive compensation and benefits; long-term incentive programs eligibility.
  • Paid time off, medical/dental/vision insurance, 401(k).
  • Equal opportunity employer; supportive, inclusive work environment.
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