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Document Specialist

Canada, Remote · Job Posted January 13, 2026
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Job Description

As a Medical Writer at Parexel, your strong scientific knowledge, writing skills, and patient focus effectively communicate complex scientific data to various stakeholders, including regulatory agencies, medical professionals, and the general public. You must be able to collaborate within cross-functional teams to achieve the development of a wide range of clinical research documents, such as model informed consent forms, clinical study reports, pharmacovigilance documents, and more.

Job Responsibility

  • Compile appendices to clinical study reports in compliance with appropriate regulatory requirements
  • Work with internal or external Clinical and/or Project Leadership functions to ensure that appendix documentation is complete and complies with the relevant guidelines
  • Use departmental publishing software to produce electronic deliverables
  • Perform MS Word formatting of clinical documents according to SOP/client/regulatory requirements
  • Coordinate production and distribution of draft and final documents to project team and client
  • Organize and track delivery of all deliverables
  • Ensure that all work is complete and of high quality prior to delivery
  • Provide support on software and document related issues to MWS staff as required
  • Ensure document is submission ready as per the appropriate regulatory guidelines
  • Provide review of draft and final documents prepared by other DS before internal or external distribution
  • Serve as contact for compilation and publishing projects, supports negotiating deliverable timelines, and resolving project-related issues
  • Serve as the Document Specialist representative on assigned project
  • Perform collection of documentation for assembly of project files and client deliverables
  • Attend and complete mandatory, corporate, project-specific, and departmental training as required
  • Assist in the training/mentoring of new departmental staff as required
  • Attend departmental and company meetings as necessary
  • Comply with departmental procedures and requirements
  • Provide administrative support if requested

Requirements

  • Primary degree or a regionally acceptable equivalent qualification, either in health-related sciences with significant experience in document processing/publishing, and/or in computer science or technology
  • Good knowledge of word processing and publishing software with proven ability (15-17 pages per hour of formatting and post PDF work)
  • Experience with processing multiple clinical documents of varying complexity such as clinical trial submission dossiers, clinical study reports, etc., as an independent document technologist or specialist
  • Excellent interpersonal, verbal and written communication skills, and good degree of initiative
  • Client focused approach to work
  • Flexible attitude with respect to work assignments and new learning
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
  • Ability to work in a matrix environment and to value the importance of teamwork
  • Advanced word processing skills in MS Word/Office
  • Advanced PDF processing skills in Adobe Acrobat
  • Advanced skills in other document editing software
  • Proficient in document management systems and key publishing software
  • Proficiency in basic grammar, punctuation, and spelling
  • Understanding of medical and pharmaceutical terminology desired
  • Advanced keyboard skills

Nice to have

ISI toolbox experience

What we offer

  • Continuous learning from being mentored to job shadowing, job rotation, and stretch assignments, as well as becoming a mentor or leading a team
  • Development and promotion based on global standards and your personal development plan
  • Patient-focused in everything we do
  • Supportive and inclusive environment
  • Career growth and development
  • Mentorship
  • Flexible work
  • Diverse projects
  • Culture of excellence
  • Global exposure

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