TSP, a Syneos Health company, seeks an Associate Director, Medical Writing to lead regulatory and clinical writing across the US, UK and EU. You will author, review, and coordinate high-quality documents to support regulatory submissions and clinical development while ensuring ICH/GCP compliance.
Reporting to the Vice President, Regulatory Affairs, you will drive strategic document development, mentor writers, and partner with cross-functional teams and vendors to interact with FDA, EMA, MHRA
#J-18808-Ljbffr