Study Feasibility Director

At AbbVie we are a company that takes on the world’s toughest health challenges. We do more than treat disease with breakthrough medicines—we aim to make a remarkable impact on people’s lives. We are a highly focused, research-driven biopharmaceutical company with over 45,000 passionate, collaborative employees around the world dedicated to scientific discovery and innovation, operational excellence, safety, and patient support.  

As a Study Feasibility Director, you will be part of AbbVie’s Clinical Development Operations (CDO) function, which is responsible for running clinical trial operations around the world.

In this role you will partner with and advise study teams on design feasibility and certain aspects of design strategy, including country and site selection, protocol review and assessment of patient burden, and related implications for patient recruitment and study timelines. This is a highly collaborative and analytical role, which will rely on your expert facilitation skills, your ability to influence without authority, and your strong experience in clinical study design, operations, and management.