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AbbViePosted 1 month ago

Head of Asset in GU, Oncology Clinical Development

$248,000–$471,500 year

HybridNorth Chicago, Illinois, United States

Full TimeSenior LevelEnterprise

Job Summary

Lead clinical development programs in GU oncology by directing design, analysis, and reporting of protocols, Investigator Brochures, and regulatory submissions. Manage a team of Medical and Scientific Directors, overseeing study integrity, enrollment timelines, and serious adverse event reporting. Chair Clinical Strategy Teams to develop vetted development plans and serve as the in-house clinical expert for key molecules, coordinating with Medical Affairs and Commercial on opinion leader interactions. Ensure compliance with Good Clinical Practices and global regulatory requirements while mentoring staff through career development initiatives.

Required Qualifications

  • Medical Doctor (M.D.), Doctor of Osteopathy (D.O.), or non-US equivalent of M.D. degree with relevant therapeutic specialty in an academic or hospital environment
  • Completion of a residency program
  • At least 7 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent
  • Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in development of clinical strategy and the design of study protocols
  • Must possess excellent oral and written English communication skills
  • Ability to exercise judgment and address complex problems and create solutions across multiple projects
  • Ability to run a complex clinical research program independently
  • Proven leadership skills and ability to bring out the best in others on a cross-functional global team
  • Must be able to lead and manage through influence
  • Demonstrated commitment to training and development of junior-level staff, using best judgment to assure that they work with an appropriate level of autonomy
  • Ability to interact externally and internally to support a global scientific and business strategy
  • Ability to interact externally and internally to support a global scientific and business strategy

Desired Qualifications

  • Completion of a subspecialty fellowship
  • 9+ years of clinical trial experience in the pharmaceutical industry, academia, or equivalent

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