Elevate your career as a Medical Writer supporting Clinical Research Scientists and Academic partners. This role involves writing regulatory documents, researching, and ensuring scientific integrity in all communications.As a Medical Writer, you'll deliver writing services to diverse stakeholders, including Sponsors and Corporations. Your work will encompass preparing and reviewing essential documents like protocols and clinical study reports, aligning with industry standards. You'll manage project timelines and have the prospect to contribute to basic training materials,



ensuring effective communication of complex scientific information.Key Responsibilities:Lead the development of regulatory documents and presentationsCoordinate with authors to finalize specialized contentTrack progress on writing projects and produce updatesConduct quality control reviews of documents as neededLiaise with publication specialists and external contactsRequirements:Bachelor's degree with 3-5 years in medical writingExperience in developing clinical documents like ICFsKnowledge of GCP, GDPR, and HIPAA regulationsProficient in EndNote/reference softwareUnderstanding of ICH M11 and AMA Style GuideContribute your expertise in medical writing to create high-quality documents that meet strict regulatory standards.

📌 Medical Writer For Clinical Research (Montreal)
🏢 Alimentiv
📍 Montreal