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 Associate 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.   

Core Responsibilities:

•     Facilitates cross-functional clinical study team interactions to assess overall design and operational feasibility.

•     Conducts detailed scientific, analytical, and operational analyses to prepare for and support study team engagements.

•     Provides scientific and strategic consultation on country strategy, site selection, protocol and patient burden, recruitment, and timelines.

•     Designs, prepares, and runs cross-functional meetings and forums to be effective and for clear outcomes. 

•     Identifies and analyzes important connections within and across therapeutic areas to optimize study performance at the portfolio level.

•     Leads and manages projects to continuously improve Study Feasibility & Enablement capabilities and impacts.

Important Competencies:

•            Strategic, agile thinking

•            Complex problem solving

•            Confident presence and strong communications

•            Cross-functional facilitation 

•            Leading through influence

•            Natural collaboration

•            Detail and analytic orientation 

• Minimum of 8 years of pharmaceutical related experience with at least 5 years in clinical research/project leadership.
•   Drug development and/or scientific project leadership experience preferred
•  Therapeutic area background in Oncology, Neurology, or Immunology preferred      
•  Strong working knowledge of pharma drug development processes
•   Recognized contributor in complex scientific analyses and decision making
• Demonstrated leadership skills with broad scientific, strategic, and business orientations