MMS is a data-focused CRO seeking a Medical Writer to critically evaluate literature, craft regulatory documents, and manage writing projects with minimal supervision. You will author protocols, briefs, study reports, consent forms, and safety summaries for regulatory submissions.
The role requires 6+ years in regulatory writing, leadership experience, and solid MS Word skills. A PhD or Masters is preferred; collaboration with global teams is essential.
📌 Senior Medical Writer (Calgary)
🏢 MMS
📍 Calgary
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