Senior Medical Writer - Regulatory Documentation
MMS
MMS, a data-focused CRO, is seeking a Medical Writer to critically evaluate literature and prepare regulatory and clinical development documents, including protocols, investigator’s brochures, and study reports. The role requires leadership in writing projects, mentoring colleagues, and coordinating with clients to meet tight deadlines. Ideal candidates will have 3+ years in pharma, strong regulatory writing experience, and advanced MS Office skills. #J-18808-Ljbffr MMS
Vacancy posted 5 days ago
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