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Job Description

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 (https://www.tiktok.com/@abbvie) .
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 advancing clinical development objectives. There is cross-functional collaboration with partners, including but not limited to clinical development, quality assurance, technology, data management, and regulatory affairs.
Study Management Associate Organization: The Study Management Associate Organization (SMAO) is responsible for supporting the Study Project Manager with the planning, execution, and oversight of clinical studies or trials. SMAO covers activities such as protocol and informed consent development, study startup, operational logistics, vendor management, and ensuring compliance with regulatory standards throughout the study lifecycle. The group works closely with cross functional teams, including but not limited to data management, regulatory affairs, Clinical Site Management (CSM) and external partners to ensure studies are conducted efficiently, within timelines, and according to quality expectations.
Clinical Acceleration and Performance: The Clinical Acceleration and Performance (CAP) function focuses on improving the efficiency, quality, and speed of clinical trials and research operations. CAP is where AbbVie reimagines how clinical trials are run. Their mission is bold but clear: deliver medicines to patients faster by making trials smarter, simpler, and more effective. The team tackles the toughest challenges in R&D—patient recruitment, site engagement, trial efficiency—by combining data science, innovative technology, and deep clinical expertise. The group is comprised of out-of-the-box thinkers, problem-solvers, and change-drivers who thrive on collaboration and creativity.
Qualifications
Minimum Qualifications:
Pursuing a Bachelor’s degree in a STEM discipline with an emphasis on Science
Expected graduation date between December 2025 – June 2026
Must be willing to relocate to AbbVie’s corporate headquarters in north suburban Chicago
Preferred Qualifications:
Proven track record of teamwork, adaptability, innovation, and integrity
Excellent communication, leadership, project management skills, problem solving, analytical skills, and business mindset
Microsoft Excel or other database experience is a plus
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ?
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. ?
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.?
This job is eligible to participate in our short-term incentive programs. ?
This job is eligible to participate in our long-term incentive programs?
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Salary: $64,000 - $122,000
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