Global Study Feasibility Director

AbbVie; New Jersey; On-site; USD 170,000 - 210,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k) plan

Paid time off

Job summary

AbbVie 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 AbbVie 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.

Qualifications

• Minimum 8 years of pharmaceutical-related experience with at least 5 years in clinical research/project leadership.
• Degree in pure, applied, or technical sciences preferred.
• Therapeutic area background in Oncology, Neurology, or Immunology preferred.

Responsibilities

• Designs, prepares, and facilitates cross-functional global strategy discussions with AbbVie leaders to assess feasibility and execution.
• Supports strategic planning for global Phase 2/3 trials with potential international scope.
• Manages matrix teams to drive analytics and recruitment planning across AbbVie functions.
• Performs scientific, analytical, and operational analyses to support study engagements.
• Provides consultation on country strategy, site selection, protocol and patient burden, recruitment and timelines.
• Leads projects to improve Study Feasibility & Recruitment capabilities.

Skills

Cross-functional leadership

Facilitation skills

Analytical

Study design

Country/site strategy

Education

Bachelor’s or advanced degree in sciences

Job description

AbbVie 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 AbbVie 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.