Medical Writer

1 week ago

Edmonton, Alberta, Canada Translational Research in Oncology Full time

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to bringing the cancer treatments of the future to the patients of today.

TRIO is seeking a Medical Writer to join our Medical Writing and Training team. This position reports to the Medical Writing Manager and is home-based in Canada.

This position is a fixed-term role starting on March 2, 2026, and ending at the end of August 2026.

Responsibilities: 

  • Prepare, edit, and finalize trial-related documents, including:
    • Clinical Trial Protocols and Synopses
    • Clinical Study Reports
    • Patient Narratives
    • Safety Update Reports
    • Abstracts and Manuscripts for publication
  • Coordinate document-related meetings, including agendas and minutes.
  • Ensure documents meet timelines, regulatory guidelines (ICH), SOPs, and sponsor requirements.
  • Perform quality control checks and address findings.
  • Maintain and update SOPs and templates for medical writing deliverables.
  • Collaborate on data analysis and interpretation to ensure accuracy in documents.
  • Submit abstracts, presentations, and manuscripts to conferences or journals.
  • Stay current with industry standards and regulatory requirements.
  • Suggest process improvements to enhance quality and efficiency.
Qualifications:
  • Bachelor's degree in a medical-related field or life sciences (post-graduate degree preferred).
  • 3-5 years of experience as a medical writer, including clinical trial documents.
  • Strong ability to write clear, accurate, and engaging medical/scientific content for diverse audiences.
  • Proven experience managing multiple trials and related documentation.
  • Solid understanding of clinical research concepts, ICH guidelines, and drug development processes.
  • Familiarity with statistical principles applied to clinical trials.
  • Strong communication and collaboration skills with internal and external stakeholders.
  • Proficiency in Microsoft Office and reference management tools.
  • Native English speaker or highly proficient in English.
  • Must be legally authorized to work in the country.

What TRIO Offers:

  • Annual compensation review and opportunities for growth
  • 3 weeks vacation plus 
  • 10 paid personal/sick days and 1 paid volunteer day per year
  • Comprehensive benefits (Health, Dental, Vision & Life Insurance) with premiums paid by TRIO
  • Up to 5% RRSP matching and optional TFSA program
  • Flexible work hours and monthly internet allowance for remote work
  • Opportunity to work out of country for short periods each year
  • Maternity/Parental leave top-up program
  • Employee Assistance Program for you and your family

Pay Range: $95,000.00 to $107, Salary will be determined based on education, experience, location, knowledge, skills, and abilities of the applicant, as well as internal equity and market alignment.

 

Prior to applying please review TRIO's Applicant Information Notice

Teamwork · Passion · Integrity · Innovation

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