Principal Regulatory Medical Writer - Client Dedicated - Canada
Fortrea(18 days ago)
About this role
Fortrea is seeking an experienced Principal Regulatory Medical Writer to lead the development of complex clinical regulatory documents for a top global pharmaceutical client. The role involves strategic input, project leadership, and collaboration across international teams to support regulatory submissions. This position offers the opportunity to work closely with high-profile clients in a dynamic environment.
Required Skills
- Regulatory Writing
- eCTD
- Clinical Documents
- Regulatory Submissions
- Medical Writing
- Clinical Study Reports
- CTD Modules
- Project Management
- Global Regulatory
- Document Development
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
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