Medical Writer

TLDR

Provide medical writing services, coordinating regulatory document production while managing timelines and quality control to support clinical research scientists and academic partners.

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

    Alimentiv delivers specialized clinical research and data services to the healthcare sector, with a strong emphasis on quality assurance and compliance. Our innovative solutions cater to the pharmaceutical and biotechnology industries, accelerating biomarker and drug development through our state-of-the-art lab and clinical imaging software.

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    Salary
    CAD $69,000 – CAD $115,500 per year
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