Senior Medical Writer — Regulatory Leader & Mentor
MMS
MMS is a data-focused CRO seeking an experienced Medical Writer to craft regulatory and clinical development documents. The role involves leading writing projects, mentoring junior writers, and coordinating directly with clients on study designs and submissions. The candidate should have 3–5 years in regulatory/clinical writing, strong MS Office skills, and a solid understanding of GCP/ICH guidelines. This is an on-site position in Atlanta, with opportunities to contribute to multi-asset therapy #J-18808-Ljbffr MMS
Vacancy posted 1 day ago
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