Elevate your career as a Lead Medical Writer with ICON, where integrity and collaboration are paramount. Oversee high-quality regulatory documents that drive current medicines to patients faster.As a Principal Medical Writer, you will manage medical writing workstreams while ensuring adherence to timelines and quality standards. This role requires expertise in preparing clinical study reports and protocols, while collaborating with clinical research, biostatistics, and regulatory teams.



Mentoring junior writers and staying updated on regulatory trends will also be crucial in your responsibilities.Key Responsibilities:Prepare and review clinical study reports accuratelyCollaborate with cross-functional teams for effective document developmentProvide guidance on best medical writing practicesMentor junior medical writers to build expertiseAct as lead writer for complex regulatory submissionsRequirements:Bachelor's degree in life sciences or related fieldSignificant medical writing experience in regulatory submissionsStrong understanding of industry standardsExceptional writing and editing skillsExcellent communication and collaboration abilitiesBring your medical writing expertise to ICON and influence the future of patient care.#J-18808-Ljbffr

📌 Lead Medical Writer At Icon (Montreal)
🏢 ICON Strategic Solutions
📍 Montreal