MMS is a data-focused CRO delivering regulatory and clinical writing support across pharmaceutical, biotech, and medical device sectors. The Medical Writer will critically evaluate literature, write and edit pivotal regulatory documents, and mentor junior writers to ensure high-quality submissions.
Responsibilities include managing timelines, coordinating with clients, and applying expert knowledge of ICH/GCP standards to multiple modules and study reports.
📌 Senior Medical Writer — Regulatory Submissions & Leadership (Calgary)
🏢 MMS
📍 Calgary