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?

A university degree in a life sciences discipline such as Medicine, Pharmacy, Bioengineering, Molecular Biology & Genetics, Chemical Engineering, Chemistry, Biology, or a related field
Fluency in English
Solid knowledge of GCP and clinical research requirements
Strong proficiency in Microsoft Word, Excel, and PowerPoint
Excellent project management, communication, and time management skills
A collaborative mindset and the ability to work effectively with internal and external stakeholders
Preferably a minimum of 2 years of industry experience in clinical study conduct
Exposure to clinical research and participation in clinical study activities
Demonstrated core and technical competencies in CRA-related or similar clinical research roles

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.

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