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 presentations
- Coordinate with authors to finalize specialized content




- Track progress on writing projects and produce updates
- Conduct quality control reviews of documents as needed
- Liaise with publication specialists and external contacts Requirements:
- Bachelor’s degree with 3-5 years in medical writing
- Experience in developing clinical documents like ICFs
- Knowledge of GCP, GDPR, and HIPAA regulations
- Proficient in EndNote/reference software
- Understanding of ICH M11 and AMA Style Guide Contribute your expertise in medical writing to create high-quality documents that meet strict regulatory standards.

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