As a Medical Writer, you will author study-level documents, including protocols, subject information, and clinical study reports. You will interpret and summarize data, drive discussions, and incorporate project strategies into documents. The role requires experience in writing regulatory documents for pharma or CRO and strong communication skills.
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As a Principal Medical Writer, you'll develop and author clinical and regulatory documents, ensuring compliance with regulatory guidelines and company standards. You'll collaborate with cross-functional teams to interpret clinical data, mentor junior writers, and contribute to developing templates and style guides. Staying current with industry trends and regulatory changes to integrate best practices into medical writing processes is expected.