Senior Medical Director, Hematology Clinical Development

Added
5 days ago
Type
Full time
Salary
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Related skills

gcp pharmacovigilance regulatory submissions clinical development clinical study reports

๐Ÿ“‹ Description

  • Oversees direction, planning, execution, and interpretation of clinical trials for development
  • Leads design/implementation of programs aligned with Product Development Plan.
  • Ensure study integrity; interpret safety/efficacy data for molecule.
  • Manage study enrollment timelines and key deliverables; report SAEs per policy.
  • Provide in-house clinical expertise; coordinate translational strategies as needed.
  • Stay updated on regulatory requirements and GCP standards.

๐ŸŽฏ Requirements

  • MD/DO or non-US equivalent; residency preferred; subspecialty fellowship desirable.
  • At least 2 years of clinical trial experience in pharma/academic.
  • Ability to run a cross-functional global clinical research program.
  • Ability to interact to support global scientific/business strategy.
  • Knowledge of trial methodology and regulatory/compliance requirements.
  • Excellent oral and written English communication skills.

๐ŸŽ Benefits

  • Comprehensive benefits: PTO, medical/dental/vision insurance, 401(k).
  • Eligible for long-term incentive programs.
  • AbbVie is an equal opportunity employer.
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