Executive Medical Director, Oncology Clinical Development

ABBVIE

South San Francisco (CA)

On-site

USD 234,000 - 444,000

Full time

10 days ago

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Job summary

AbbVie invites applications for an Executive Medical Director in Oncology Clinical Development (Solid Tumors). This full-time role leads the direction and execution of clinical trials, coordinating cross-functional teams and ensuring high-quality data and regulatory compliance.

The candidate should have an MD/DO (or international equivalent), 5–7 years of trial experience, and strong leadership with excellent English communication.

Qualifications

  • MD or DO or non-US equivalent with relevant specialty.
  • Residency completion strongly preferred; subspecialty fellowship desirable.
  • At least 5 years (7 years preferred) of clinical trial experience in pharma, academia, or equivalent.
  • Ability to run a complex clinical research program independently.
  • Proven leadership and ability to lead cross-functional global teams.
  • Excellent oral and written English communication skills.

Responsibilities

  • Lead design, analysis, interpretation, and reporting of protocols and regulatory submissions.
  • Oversee clinical study teams, monitor study integrity, and review safety/efficacy data.
  • Chair Clinical Strategy Team(s) and develop a rigorous Clinical Development Plan.
  • Serve as in-house clinical expert, coordinating with stakeholders across functions.
  • Ensure adherence to Good Clinical Practices and regulatory standards.
  • Represent AbbVie at external meetings as required.

Skills

Leadership
Cross-functional collaboration
Strategic thinking
Communication skills

Education

MD/DO or international equivalent

Job description

AbbVie invites applications for an Executive Medical Director in Oncology Clinical Development (Solid Tumors). This full-time role leads the direction and execution of clinical trials, coordinating cross-functional teams and ensuring high-quality data and regulatory compliance.

The candidate should have an MD/DO (or international equivalent), 5–7 years of trial experience, and strong leadership with excellent English communication.

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