Senior Regulatory Medical Writer & Team Lead
MMS
MMS is a global CRO focused on data-driven regulatory writing for pharmaceutical clients. The Medical Writer will evaluate literature, draft protocols, study reports, consent forms, and safety summaries, ensuring scientific rigor and regulatory compliance. With 3+ years in regulatory writing, you will mentor junior writers, coordinate with clients, and manage timelines under tight schedules. Strong MS Word and presentation skills are essential in a collaborative, fast-paced environment in San #J-18808-Ljbffr MMS
Vacancy posted 3 days ago
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