Clinical Feasibility Lead – Study Design and Analytics

ABBVIE; South San Francisco (CA); On-site; USD 110,000 - 209,000; Full time

Job summary

AbbVie in South San Francisco, CA is seeking a Feasibility Manager in Study Feasibility to partner with study teams on design feasibility, country and site selection, and patient recruitment timelines.

The role requires strong background in clinical study design, operations, and management, with the ability to influence without authority, and to lead cross-functional initiatives across global trials.

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.
• Reviews metrics and escalates issues to Feasibility AD/Directors.
• Incorporates insights from 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.

Education

Bachelor’s Degree, preferably in pure, applied, or technical sciences

Job description

AbbVie in South San Francisco, CA is seeking a Feasibility Manager in Study Feasibility to partner with study teams on design feasibility, country and site selection, and patient recruitment timelines.

The role requires strong background in clinical study design, operations, and management, with the ability to influence without authority, and to lead cross-functional initiatives across global trials.