Manager, Study Feasibility

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

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

Requirements

Bachelor’s Degree, preferably in pure, applied, or technical sciences; 6+ years of experience in drug development and/or clinical trial operations; Drug development and/or scientific project leadership experience preferred; Strong working knowledge of pharma drug development processes; Experience with complex scientific analyses and decision making; Demonstrated leadership skills with broad scientific, strategic, and business orientations