Global Study Feasibility Director

Allergan; Irvine (CA); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Comprehensive benefits package

401(k) plan

Paid time off

Job summary

AbbVie seeks a Study Feasibility Associate Director to lead global strategy for clinical trial feasibility and design decisions. You will influence country/site selection, patient burden assessments, and recruitment timelines while partnering with study teams across therapeutic areas.

The role emphasizes collaborative leadership, expert facilitation, and a track record in study design, operations, and management within pharma. Expect international collaboration and strategic impact.

Qualifications

• Minimum 8 years of pharmaceutical experience with at least 5 years in clinical research/project leadership.
• Experience guiding study design, country/site strategy, and recruitment planning.
• Strong ability to analyze complex data and advise senior teams.

Responsibilities

• Designs, prepares, and facilitates cross‑functional global strategy discussions.
• Supports strategic planning for large global phase 2 and 3 trials across 35+ countries.
• Manages matrix leadership to drive insights and recruitment planning.
• Conducts detailed scientific, analytical, and operational analyses.
• Provides consultation on country strategy, site selection, and timelines.
• Identifies connections across therapeutic areas to optimize portfolio performance.
• Leads projects to improve Study Feasibility & Recruitment capabilities.

Skills

Clinical project leadership

Analytical thinking

Leadership

Pharma development knowledge

Strategic consulting

Education

Bachelor’s or advanced Degree in sciences

Job description

AbbVie seeks a Study Feasibility Associate Director to lead global strategy for clinical trial feasibility and design decisions. You will influence country/site selection, patient burden assessments, and recruitment timelines while partnering with study teams across therapeutic areas.

The role emphasizes collaborative leadership, expert facilitation, and a track record in study design, operations, and management within pharma. Expect international collaboration and strategic impact.