Step into a Clinical Research Medical Writer role focused on developing high-quality regulatory documents. Your expertise will guide collaboration with scientists and external experts, driving the accuracy of research submissions.This role demands a solid 3-5 years of medical writing experience, particularly in producing protocols, informed consent forms, and clinical study reports. You will ensure that all deliverables meet established standards while tracking their progress and managing timelines of multiple projects.Key Responsibilities:Lead the production of regulatory documentation across projectsCollaborate with technical specialists for content accuracyManage projects by tracking deliverable timelinesParticipate in quality reviews for author contributionsSupport editing and proofreading of study-related documentsRequirements:Minimum undergraduate degree, advanced degrees preferred3-5 years of related medical writing experienceKnowledge of GCP, GDPR, and HIPAA regulationsProficient in EndNote/reference software for citation managementStrong communication skills, with an ability to work diplomaticallyUse your medical writing talent to support vital clinical research initiatives in this resourceful position.

📌 Clinical Research Medical Writer (Toronto)
🏢 Alimentiv 2
📍 Toronto