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.
We are looking for a motivated and collaborative team member who combines scientific curiosity with operational discipline, and who is eager to contribute to high-quality clinical research in a fast-paced, collaborative, and purpose-driven environment to support our Medical Operations processes, particularly within non-interventional studies. Depending on the candidate’s experience, qualifications, and overall assessment, this role may be positioned at the Assistant CRA, CRA, or Senior CRA level.
In this role, the successful candidate will be responsible for managing study sites, in studies overseen by Medical Operations, including but not limited to AbbVie sponsored non-interventional studies, investigator-initiated studies, and collaborative research. The role involves ensuring that all activities are conducted in accordance with relevant processes, procedures, and applicable local laws and regulations, while supporting the timely and high-quality delivery of data within agreed parameters.
In this role, you will play a key part in the planning, coordination, oversight, and delivery of clinical study activities, ensuring they are conducted in accordance with applicable processes, procedures, local regulations, and quality standards. You will support the successful execution of studies from initiation through close-out, with responsibility for maintaining data quality, operational excellence, and compliance throughout the study lifecycle.
You will work closely with the Medical Operations Manager and cross-functional stakeholders to support essential study activities, including site selection, initiation, monitoring (if required), close-out, investigator meetings, regulatory and ethics submissions, vendor coordination, and study documentation management. The role also involves proactively identifying risks and issues, escalating them appropriately, and contributing to timely corrective and preventive actions to support study integrity and delivery.
The successful candidate will demonstrate strong ownership, sound judgment, and the ability to build effective partnerships across internal and external stakeholders. This position offers the opportunity to contribute to meaningful scientific work within a dynamic environment, where quality, compliance, and collaboration are fundamental to success.
What we are looking for?
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
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.
Learn more about us at www.abbvie.com and review our community guidelines at https://www.abbvie.com/social-media-community-guidelines.html.
