As a Feasibility Manager in Study Feasibility, 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 strong experience in clinical study design, operations, and management, and may require your ability to influence without authority.

Responsibilities

• Manages reporting of Feasibility Team Portfolio deliverables and contribution to organizational performance targets
• Reviews metrics and escalates issues to Feasibility AD/Directors
• Incorporates insights from across 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