2026 Clinical Trial Operations Development Program
AbbVieAbout the role
Company Description
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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
Clinical Trials are required before a new compound can be available for use by patients. A clinical study in human volunteers is conducted to answer specific health questions: Is it safe? Does it work? Is it better than what is currently offered to patients? At AbbVie, the Clinical Operations group conducts/manages clinical trials and provides therapeutically aligned, scientific strategy and operations management for the planning, execution and reporting of clinical development programs to enable successful global registration and commercialization of drug development projects.
As a member of AbbVie’s Clinical Trial Operations Development Program (CTODP), you will participate in two 12-month rotational assignments over the course of two years. The rotations offer global exposure to Clinical Operations leadership and are crafted to help members hone exceptional functional and leadership traits. Members will develop expertise, skills, and relationships essential for accelerated career progression within Clinical Operations.
Robust and meaningful rotational assignments will be hosted in the following three areas:
- Clinical Data Strategy & Operations: The Clinical Data Strategy Operations (CDSO) function is responsible for overseeing and executing against the strategy around clinical data collection, management, integration, and utilization within AbbVie clinical trials. This includes the operations and technology to enable data acquisition, quality assurance, governance, compliance, data architecture, and effective data analysis to support decision-making. The organization works to ensure clinical data is robust, accurate, and usable for regulatory submissions, evidence generation, and ad
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