Senior Medical Director, Oncology Early Development

Added
8 days ago
Type
Full time
Salary
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Related skills

clinical development clinical study reports regulatory compliance good clinical practice
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📋 Description

  • Oversees direction, planning, execution, and interpretation of clinical trials or research
  • Participates in cross-functional teams to generate high-quality clinical data supporting product
  • Designs and implements clinical development programs aligned with regulatory requirements and
  • Oversees study enrollment, timelines, and data safety/efficacy assessments in collaboration with
  • Provides clinical expertise for molecule/disease, coordinating with internal stakeholders and

🎯 Requirements

  • Medical Doctor (M.D.), D.O., or non-US MD-equivalent with relevant specialty. Residency and
  • At least 2 years of clinical trial experience in pharma, academia, or equivalent.
  • Ability to lead a cross-functional global clinical research program with minimal supervision.
  • Strong collaboration, communication, and regulatory knowledge for global development.
  • Excellent English oral and written communication skills.

🎁 Benefits

  • AbbVie comprehensive benefits package and competitive compensation.
  • Eligibility for long-term incentive programs.
  • Equal opportunity employer; commitment to integrity and inclusion.
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