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 strong MS Word skills. A PhD or Masters is preferred; collaboration with global teams is essential.
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Senior Medical Writer & Regulatory Submissions Lead in Calgary employer: MMS
MMS is recognized as a Great Place to Work certified organization, highlighting its exceptional culture and industry-leading employee retention rate. The company fosters a collaborative and inclusive work environment, providing opportunities for professional growth and development. Employees are part of a supportive team that values their contributions and is dedicated to shaping the future of clinical research.
