Executive Medical Director, Oncology Clinical Development

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30 minutes ago
Type
Full time
Salary
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Related skills

gcp leadership pharmacovigilance oncology regulatory
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📋 Description

  • Lead design, execution, and interpretation of clinical trials across programs.
  • Own cross-functional teams to deliver high-quality clinical data.
  • Oversee study teams, timelines, and data safety assessment.
  • Lead regulatory interactions and ensure GCP compliance.
  • Contribute to translational strategies and due diligence as needed.

🎯 Requirements

  • MD/DO or equivalent with oncology subspecialty desirable.
  • 5+ years in clinical development; 7+ preferred.
  • Proven leadership in cross-functional global teams.
  • Strong knowledge of trial methodology and regulatory requirements.
  • Ability to interact with external partners and internal stakeholders.
  • Experience in study protocol design and regulatory submissions.

🎁 Benefits

  • Competitive compensation with annualized range based on location.
  • Comprehensive benefits package and long-term incentive programs.
  • Equal opportunity employer; includes veterans and disabled.
  • Participation in 401(k) and related employee programs.
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