Oncology Clinical Development Director - Solid Tumors

Allergan

North Chicago (IL)

On-site

USD 180,000 - 240,000

Full time

4 days ago
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Benefits offered by this job

Paid time off
Medical/dental/vision insurance
401(k) plan

Job summary

AbbVie seeks a clinical development physician to supervise study design, execution, and interpretation within a global program. You’ll ensure compliance with GCP and regulatory standards while coordinating with Medical Affairs, Clinical Operations, and cross-functional partners.

The role emphasizes data integrity, protocol development, and timely communication of findings to support product strategy. Prior experience in pharma or academic settings is preferred.

Qualifications

  • Medical doctor with relevant specialty and residency training.
  • Experience leading or overseeing clinical trials in pharma/academia.
  • Strong understanding of trial methodology and regulatory requirements.
  • Excellent oral and written English communication.
  • Ability to collaborate across multiple functional teams.

Responsibilities

  • Design and implement study protocols for a clinical development program.
  • Oversee study integrity, monitoring safety and efficacy data.
  • Contribute to data analysis, reporting, and regulatory submissions.
  • Participate in Clinical Strategy Teams and cross-functional alignment.
  • Engage with investigators and study staff; stay current with guidelines.

Skills

Clinical trials experience
Regulatory/compliance knowledge
Cross-functional collaboration
English communication
Study design knowledge

Education

M.D. or D.O. degree

Job description

AbbVie seeks a clinical development physician to supervise study design, execution, and interpretation within a global program. You’ll ensure compliance with GCP and regulatory standards while coordinating with Medical Affairs, Clinical Operations, and cross-functional partners.

The role emphasizes data integrity, protocol development, and timely communication of findings to support product strategy. Prior experience in pharma or academic settings is preferred.

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