Feasibility Study Lead — Clinical Development

Allergan; Irvine (CA); On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie in Irvine, CA, is seeking a Feasibility Manager to partner with study teams on design feasibility, country and site selection, protocol review, and patient burden assessments impacting recruitment and timelines.

This highly collaborative role requires strong experience in clinical study design, operations, and management, with the ability to influence across functions and drive continuous improvement.

Qualifications

• 6+ years of experience in drug development and/or clinical trial operations.
• Drug development and/or scientific project leadership experience preferred.
• Strong working knowledge of pharma drug development processes.
• Experience with complex scientific analyses and decision making.
• Demonstrated leadership skills with broad scientific, strategic, and business orientations.

Responsibilities

• Manages reporting of Feasibility Team Portfolio deliverables and contribution to organizational performance targets
• Reviews metrics and escalates issues to Feasibility AD/Directors
• Incorporates insights from across Feasibility & Business Insights team
• Assists Feasibility ADs/Directors in conducting detailed scientific, analytical, and operational analyses to prepare for and support study team engagements
• Identifies and analyzes important connections within and across therapeutic areas and works with Feasibility ADs/Directors to optimize study performance at the portfolio level
• Manages with ability to lead continuous improvement projects
• Strategic, agile thinking, complex problem solving, confident presence and strong communications, cross-functional facilitation, natural collaboration, detail and analytic orientation

Skills

Leadership

Education

Bachelor’s Degree in pure/applied/technical sciences

Job description

AbbVie in Irvine, CA, is seeking a Feasibility Manager to partner with study teams on design feasibility, country and site selection, protocol review, and patient burden assessments impacting recruitment and timelines.

This highly collaborative role requires strong experience in clinical study design, operations, and management, with the ability to influence across functions and drive continuous improvement.