Medical Writer

In this role you will be providing medical writing services and consultation to Clinical Research Scientists, Academic partners, Sponsors and/or the Corporation, which may include researching, writing, reviewing and editing scientific information, coordinating document reviews with authors, conducting reference searches and verifying citations, translating research data and findings into regulatory documents (protocols, investigator brochures, clinical study reports, informed consent forms, etc.) and presentations on a timely basis and in alignment with industry, regulatory and academic style and content guidelines and standards. Track progress and timelines for assigned writing projects. Perform document quality control review when requested. Assist with writing or review of relevant training materials or work instructions as needed. Clinical Research/Academic Writing Support Lead the content planning and production of regulatory documents (protocols, investigator brochures, clinical study reports, informed consent forms, etc.) in alignment with established standards and guidelines Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content (exhibits, illustrations, tables, and appendices) for publication into finished documents appropriate for the stated audience Act as the project manager for writing deliverables and regularly track timelines and provide progress reports to stakeholder(s) Participate in quality control review for documents written by other authors when requested Publication Support Act as primary contact and liaison with external publication executives, illustrators, designers, and editors, representing the Scientists/Investigators, Sponsors and/or the corporation with external specialists to select publication content, address content change requests, complete written revisions and/or resolve competing content requirements Other Writing Support Upon request, support study teams with review, editing or proof-reading of study documents or templates, such as charters, informed consent forms, or study plans (safety, statistical analysis, etc.) Assist with writing or reviewing relevant training materials or work instructions when requested Qualifications Minimum of an undergraduate degree (advanced degrees preferred) and 3-5 years of relevant experience in medical writing Previous experience leading the development of protocols, ICFs, and CSRs Trained in GCP, GDPR, and HIPAA Advanced knowledge of EndNote/reference software Familiarity with graphical software and figure development is an asset Ability to adapt to shifting priorities and assignments Highly refined written and oral communication skills Demonstrated ability to work with diplomacy and tact Previous experience/knowledge of Gastroenterology is an asset Familiarity with ICH M11 and the AMA Style Guide is an asset Continuous improvement mindset and willingness to embrace new technologies where appropriate Stay Alert to Recruitment Scams We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn’t feel right, we encourage you to verify before responding. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us. + bonus

The role involves providing medical writing and consultation services to create and edit regulatory documents such as protocols and clinical study reports. The position also acts as a project manager for writing deliverables and a liaison with external publication specialists.

Candidates must have at least an undergraduate degree and 3-5 years of relevant medical writing experience, specifically leading the development of protocols and CSRs. Proficiency in GCP, GDPR, HIPAA, and reference software like EndNote is required.

• Google CloudPreferred
• Project managementPreferred

Identified from the job description. Confirm important requirements above.

• Medical Writing
• Regulatory Writing
• Project Management
• Quality Control Review
• Clinical Study Reports
• Investigator Brochures
• Informed Consent Forms
• Reference Searching
• GCP
• GDPR
• HIPAA
• EndNote
• AMA Style Guide
• ICH M11
• Gastroenterology
• Communication Skills

• Healthcare
• Science & Research
• Manufacturing
• Creative & Media
• Management & Leadership

Minimum education

Bachelor’s degree

Minimum experience

2+ years

Apply by

Sep 23, 2026

Posting language

English

Working hours

40 hours per week

Location requirements

Country, Montreal, Quebec, Canada

Seniority

Not Applicable

Application method

Direct apply is available