Medical Writer job, CA – Katalyst HealthCares & Life Sciences.

April 5, 2017 – Medical Writer – Responsibilities: Writes clinical and regulatory documents. Initial project is to write a Phase 3 protocol in collaboration with a small study team. Additionally, the position will potentially write one or more briefing documents for regulatory agency meetings and support other medical writing projects as needed. Author, co-author, critically edit, and format clinical and regulatory documents including protocols, CSRs, Investigator Brochures, briefing documents, marketing applications, and other regulatory submissions; Manage medical writing timelines for assigned projects


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