Senior Regulatory Medical Writer - Client Dedicated - Canada

At Fortrea, we help bring life‑changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high‑complexity clinical regulatory documents in partnership with a leading global pharmaceutical company.What You Will DoAs a sponsor‑embedded Regulatory Medical Writer, you will lead the full development lifecycle of Phase II–IV clinical regulatory documents, with primary responsibility for:Clinical ProtocolsInvestigator’s Brochure (IBs)SubmissionsYou will own document development from planning through final delivery, including:Leading kick‑off, communication, and comment‑resolution meetingsCoordinating cross‑functional contributors and reviewersMaintaining alignment with sponsor goals, timelines, and milestonesInterpreting clinical data and translating results into clear, compliant regulatory documentsWho You Will Work WithYou will collaborate with global, cross‑functional teams including Biostatistics, Data Management, Prog...