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Global Study Feasibility Director

Job in Edison, Middlesex County, New Jersey, 08817, USA
Listing for: AbbVie
Full Time position
Listed on 2026-10-31
Job specializations:
  • Research/Development
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 170000 - 210000 USD Yearly USD 170000.00 210000.00 YEAR
Job Description & How to Apply Below

Abb Vie is seeking a Study Feasibility Associate Director to join Clinical Development Operations. You will design global feasibility strategies, advise on country and site selection, and coordinate across senior Abb Vie leaders to optimize study timelines and recruitment.

The role requires 8+ years in pharma, with 5+ years in clinical research leadership, and a strong background in oncology, neurology, or immunology. Competitive benefits and long-term incentives are offered.

Step into the Global Study Feasibility Director role at Abb Vie in NJ, United States and grow with us.

Please review the full job details above before applying.

If your experience matches this role, we encourage you to apply.

All applications are reviewed carefully by our team.

The position is based in NJ, United States.

This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.

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