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.
Responsibilities:
- Lead and develop Direct Reports: Managers and Associate Directors
- Leads cross-functional clinical study team, Integrated Evidence Strategy Team and Asset Strategy Team interactions to assess overall design and operational feasibility
- Conducts detailed scientific, analytical, and operational analyses to prepare for and support team engagements
- Provides scientific and strategic consultation and recommendations on country strategy, site selection, protocol and patient burden, recruitment, and timelines
- Leverages broad and deep scientific and organizational knowledge to work within and across therapeutic areas
- Identifies risks from multiple perspectives and proposes potential mitigation strategies and solutions
- 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 cross-functional initiatives and organizational change workstreams
Design and develop study, program and portfolio level feasibility tools and processes - Improves and standardizes the clinical trial development process across the portfolio