Executive Medical Director, Oncology Clinical Development

Added
5 hours ago
Type
Full time
Salary
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Related skills

gcp pharmacovigilance oncology regulatory clinical development

๐Ÿ“‹ Description

  • Leads the direction, planning, execution of clinical trials in oncology programs.
  • Participates in cross-functional teams to deliver high-quality clinical data.
  • Oversees study timelines, enrollment, safety and efficacy data interpretation.
  • Responsible for design/analysis/interpretation of protocols and regulatory documents.
  • May chair Clinical Strategy Teams and oversee investigators and staff.
  • Represents AbbVie in external meetings and ensures compliance with regulatory requirements.

๐ŸŽฏ Requirements

  • MD/DO or non-US equivalent; oncology subspecialty desirable.
  • 5+ years clinical development/trial experience in pharma or academia.
  • Ability to lead complex programs and cross-functional teams.
  • Strong leadership, external/internal collaboration, and regulatory knowledge.
  • Deep knowledge of trial methodology, regulatory/compliance standards, and study design.

๐ŸŽ Benefits

  • Competitive compensation package.
  • Comprehensive benefits including medical/dental/vision and 401(k).
  • Long-term incentive program eligibility.
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