Medical Writer

About the Opportunity Brown Consulting Group is supporting a confidential client in the search for a Medical Writer. Our client is a specialized medical communications agency that partners with pharmaceutical and biotechnology companies, healthcare professional organizations, and patient advocacy groups to develop customized, evidence-based communications that support positive changes in health behaviours and patient outcomes. About the Role The successful candidate will join a remote content team and develop accurate, engaging, and strategically aligned medical communications across therapeutic areas and audiences. Projects may include symposium content, education modules, advisory meeting materials, patient information, manuscripts, and related healthcare communications. Working closely with internal project teams, corporate clients, healthcare professionals, and vendors, the Medical Writer will create high-quality content that maintains scientific integrity, meets audience needs, and aligns with brand strategy, regulatory requirements, and applicable review standards. Key Responsibilities Navigate and select appropriate source evidence according to the project specifications, including scientific literature, conference materials, regulatory documents, funding reports, and other credible healthcare sources Create content outlines that reflect project objectives, format, scope, quality standards, timelines and budget expectations Develop evidence-based, current, accurate, and clear content tailored to the intended audience, including pharmaceutical marketing and medical teams, healthcare professionals, patients, caregivers, and lay audiences Align content with client brand strategy, messaging, style guides, compliance requirements, and regulatory standards Adhere to project-specific parameters, including accreditation standards, pharmaceutical manufacturer codes of conduct, and advertising codes Prepare audit-ready content by citing and highlighting evidence sources and building reference collections to support fact checking, reference-tagging, and formal medical-legal-regulatory (MLR) and accreditation reviews Participate in pharmaceutical client and healthcare professional faculty calls, contributing to content-related discussions as guided by project leads Support project planning, scoping, estimating, and progress tracking and reporting related to content development Collaborate with internal teams to prepare project communications, status updates, and project-related collateral materials (e.g., invitations, online surveys, event guides) Contribute to the execution of virtual and in-person programs, including program set-up, note-taking duties, faculty assistance and client customer service support when required Identify opportunities to improve quality, efficiency, processes, and day-to-day workflows Qualifications Graduate degree in life sciences, health sciences, or a related field. 1 – 3 years medical writing experience, ideally related to biopharmaceutical agents, disease treatment, in healthcare, pharmaceutical, agency, clinical, or marketing environments. Experience in the oncology space is an asset. Strong ability to critically appraise medical literature and apply principles of evidence-based medicine, including a solid understanding of clinical trial design, eligibility criteria, endpoint selection and data interpretation. Ability to identify and digest therapeutic area-focused resources, including disease management guidelines and treatment protocols, and follow decision-making along patient journeys and care paths. Skill in developing scientifically rigorous content while maintaining clarity, conciseness, story flow, and audience relevance. Familiarity with and aptitude for applying regulatory, medical-legal, accreditation, and external review guidance, including the Pharmaceutical Advertising Advisory Board (PAAB) code, and pharmaceutical company MLR requirements. Strong command of professional English, including grammar and vocabulary, with ability to deliver a polished, audience-appropriate tone in both written and spoken communication. Confidence communicating in virtual and in-person settings with internal colleagues, corporate clients, healthcare professionals, and vendors. Curiosity, sound judgment, and a willingness to ask thoughtful questions, challenge assumptions, seek feedback, and stay current with industry trends and best practices. Strong organizational skills and the ability to follow timelines, track progress and time on task, and contribute to discussions about project-related costs and other requirements. Technical Skills High proficiency with Microsoft Office, including Outlook, Excel, Word, PowerPoint, Teams, and SharePoint. Familiarity with AMA referencing style. Working knowledge of reference management tools such as Zotero, Mendeley, or EndNote. Experience with time tracking tools; Blue Memento experience is an asset. French written and spoken communication skills are an asset. How to Apply If you are a curious, evidence-driven medical writer who enjoys translating scientific information into impactful healthcare communications, Brown Consulting Group would welcome your application. Please submit your resume and a brief cover letter outlining your relevant medical writing experience. No phone calls or solicitation, please. We thank all candidates who apply, however, only those chosen for an interview will be contacted.

The Medical Writer will develop accurate and engaging medical communications across various therapeutic areas while collaborating with internal teams and clients. Responsibilities include creating content outlines, aligning content with brand strategy, and preparing audit-ready materials.

Candidates should have a graduate degree in life sciences or a related field and 1-3 years of medical writing experience, preferably in biopharmaceuticals. Strong skills in critical appraisal of medical literature and familiarity with regulatory requirements are essential.

• Gestion de projetSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Medical Writing
• Evidence-Based Medicine
• Content Development
• Scientific Literature
• Regulatory Compliance
• Project Management
• Communication Skills
• Critical Appraisal
• Oncology Knowledge
• Microsoft Office
• Reference Management
• Curiosity
• Organizational Skills
• Team Collaboration
• Client Interaction
• Healthcare Communication

• Healthcare
• Marketing
• Consulting
• Science & Research
• Creative & Media

Formation minimale

Maîtrise

Expérience minimale

2+ ans

Postuler avant le

21 déc. 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Niveau d’expérience

Entry level

Mode de candidature

La candidature directe est offerte