Director I, Study Feasibility
North Chicago, IL, United States Hybrid
$160,500–$305,000 a yearJobFig found this opening at its original source and checks that it remains available.
About the role
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.
What you'll bring
- Bachelor’s or advanced Degree
- Minimum of 10 years of pharmaceutical related experience, 8 years in clinical research/project leadership/consulting, 4 years in a managerial role
- Strong working knowledge of pharma drug development processes at a study, program, and portfolio level
- Recognized leader in complex scientific analyses and decision making
- Demonstrated leadership skills with broad scientific, strategic, and business orientations
- or Advanced degree (MBA, PharmD, PhD, or MD in a health care or related field) desirable with minimum of 2 years in clinical research/project leadership/consulting
- Drug development and/or scientific project leadership experience preferred
- Therapeutic area background in Oncology, Neurology, or Immunology preferred
- preferably in pure, applied, or technical sciences