Fortrea

Senior Regulatory Medical Writer

Fortrea

full-time

Posted on:

Location Type: Remote

Location: Canada

Visit company website

Explore more

✨ AI Apply
Apply

Job Level

Senior

About the role

  • Lead the development lifecycle of Phase II–IV clinical regulatory documents
  • Own document development from planning through final delivery
  • Coordinate cross‑functional contributors and reviewers
  • Interpret clinical data and translate results into regulatory documents

Requirements

  • Bachelor’s degree in life science
  • Advanced degree in life sciences (Master’s or PhD) preferred
  • Minimum 4 years of regulatory medical writing experience
  • At least 2 years as a medical writing project lead
  • Strong expertise in CSRs and Protocols
Benefits
  • Training
  • Mentorship
  • Access to a global network of experts
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
regulatory medical writingclinical regulatory documentsclinical study reports (CSRs)protocolsdata interpretation
Soft Skills
leadershipcoordinationcommunication