Senior Medical Director, Oncology Early Development

Added
9 days ago
Type
Full time
Salary
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Related skills

gcp pharmacovigilance oncology regulatory clinical development

📋 Description

  • Lead design, execution, and interpretation of early phase trials
  • Oversee cross-functional teams to deliver high-quality clinical data
  • Oversee clinical study plans, enrollment, and timelines
  • Provide in-house clinical expertise for molecule and disease areas
  • Coordinate translational strategies with Discovery colleagues
  • Ensure compliance with GCP and regulatory standards

🎯 Requirements

  • MD/DO or non-US equivalent; oncology subspecialty desirable
  • 3+ years clinical trial experience in pharma/academia
  • Ability to run moderate complexity clinical programs
  • Strong cross-functional collaboration and communication
  • Experience in thoracic malignancies or T-cell engagers preferred
  • Knowledge of trial methodology, regulatory requirements, and study design

🎁 Benefits

  • Competitive compensation and long-term incentive programs
  • Comprehensive medical/dental/vision benefits
  • 401(k) retirement plan and employee benefits
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