Job Description

As part of an RRD International, LLC project team, the Senior Clinical Research Associate (CRA) or CRA is responsible for helping to plan, initiate, maintain, and close-out clinical studies. This position primarily involves in-house support to ensure clinical trial documents and responsibilities are in compliance with all RRD Standard Operating Procedures, as well as applicable regulations and guidelines. Involves monitoring management/oversight and some monitoring or co-monitoring of clinical sites to ensure that they are in compliance with all applicable regulations and guidelines.

This position requires willingness to travel, up to 20%.


From backgrounds in pharma/biotech, CRO management and at the FDA, the RRD team delivers a unique combination of knowledge, experience and strategic thinking to product development, across all major classes and therapeutic areas.

If you would like to be a part of our world-class team, please complete the form below and attach your resume.

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