Job Description

Medical Writing Operations provides support to RRD International, LLC (RRD) medical writing and regulatory affairs operations for investigational drug, biologic, and medical device projects, including review, development, and implementation of document management procedures; quality control checks; editing and formatting; and management of standards in the publishing/compilation of documents for submission to Regulatory Health Authorities.


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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