Executive Medical Director, Oncology Early Development

AbbVie

North Chicago (IL)

On-site

USD 180,000 - 240,000

Full time

3 days ago
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Benefits offered by this job

Comprehensive benefits package
Long-term incentive programs

Job summary

AbbVie in North Chicago, IL seeks an experienced clinical development leader to direct and interpret multiple clinical trials within a development program. The role drives study design, data interpretation, regulatory submissions, and cross-functional collaboration to advance therapeutic candidates.

The ideal candidate has MD/DO with 5+ years of trial leadership, strong English communication, and a proven ability to lead through influence within global teams.

Qualifications

  • MD/DO or international equivalent with relevant therapeutic specialty.
  • Residency program completed; subspecialty fellowship desirable.
  • 5+ years of clinical trial experience in pharma, academia, or equivalent.
  • Must possess excellent oral and written English communication skills.

Responsibilities

  • Leads and demonstrates ownership of multiple clinical development programs within the overall product development plan.
  • Oversees study teams, monitors study integrity, and reports safety & efficacy data.
  • Design, analysis, interpretation, and reporting of clinical protocols and study documents.
  • May supervise Medical/Scientific Directors on related programs.
  • Collaborates across Discovery, Medical Affairs, and Regulatory to align clinical development plans.
  • Ensures adherence to Good Clinical Practices and regulatory requirements.

Skills

Leadership
Cross-functional collaboration
Strategic thinking
English communication

Education

MD/DO or international equivalent
Residency completed
Subspecialty fellowship desirable
Clinical trial experience (5+ years)

Job description

AbbVie in North Chicago, IL seeks an experienced clinical development leader to direct and interpret multiple clinical trials within a development program. The role drives study design, data interpretation, regulatory submissions, and cross-functional collaboration to advance therapeutic candidates.

The ideal candidate has MD/DO with 5+ years of trial leadership, strong English communication, and a proven ability to lead through influence within global teams.

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