16 Medical Writer jobs in Canada available for remote work from home. Apply for positions such as Medical Writer, Medical Writer, Senior Medical Writer (Remote - Canada) and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The medical writer will research, write, and edit regulatory documents such as protocols, investigator brochures, and clinical study reports while coordinating with authors and stakeholders. They will also act as a project manager for writing deliverables, ensuring adherence to industry standards and timelines.
The Medical Writer is responsible for preparing and quality-checking clinical documents, including protocols, CSRs, and scientific publications. They also handle document e-publishing and may serve as a DMC Administrator to coordinate committee meetings and charters.
The Medical Writer will critically analyze medical literature and write various clinical development documents, including protocols and study reports. They will also manage project timelines, interact directly with clients, and mentor team members throughout the writing process.
Develop and deliver high-quality, accurate scientific content for oncology-focused accounts, including manuscripts and slide decks. Provide editorial oversight, manage project timelines and budgets, and collaborate with internal teams and clients.
![Citrus Health Group, Inc is hiring for remote Senior Medical Writer [Medical Communications/Publications]](/assets/74ffa30f-0e0b-4846-98e2-52f5aab15827.jpg){kind=small}
The Senior Medical Writer is responsible for researching, writing, and editing high-quality scientific content for medical communications initiatives. They must manage project timelines, collaborate with stakeholders, and ensure all deliverables meet ethical and editorial standards.
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The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for organizing, analyzing, and presenting scientific and statistical information in compliance with ICH and regulatory guidelines.
The Principal Medical Writer independently plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing, interpreting, and presenting scientific and statistical information in compliance with ICH and regulatory standards.
The Senior Medical Writer will lead document authorship for various clinical projects and serve as a project lead for smaller engagements. They will collaborate with delivery teams to produce high-quality regulatory documents while maintaining strong client relationships.
The Senior Medical Writer will lead clinical regulatory writing projects and serve as a key contributor to document authorship across various service lines. They will interface directly with clients and support complex engagements as part of a global delivery team.
The Principal Medical Writer leads the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews, mentor junior staff, and maintain strong relationships with clients and internal departments.
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support product development. They are responsible for analyzing and presenting scientific information in accordance with industry guidelines and company standards.
Author accurate regulatory documents such as CSRs, protocols, and IBs to support clinical trial authorizations and marketing applications. Lead writing projects from initiation to close-out while managing sponsor relationships and performing peer quality reviews.
The Senior Medical Writer leads the authorship of clinical regulatory documents and manages smaller projects while supporting larger engagements. They interface directly with clients to ensure goals are met and maintain professional business relationships.
The Principal Medical Writer plans and prepares regulatory documents and medical communications to support all phases of product development. They lead project teams, author high-quality submission-level documents, and collaborate with cross-functional teams to ensure regulatory compliance.
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