Senior Regulatory Medical Writer - Client Dedicated - Canada
Fortrea(18 days ago)
About this role
Fortrea is seeking an experienced Senior Regulatory Medical Writer to lead the development of complex clinical regulatory documents for a leading global pharmaceutical company. The role involves managing document development from planning to delivery, collaborating with international teams, and translating clinical data into regulatory documents.
Required Skills
- Regulatory Writing
- Clinical Data Analysis
- Document Management
- Project Leadership
- Collaboration
- Clinical Protocols
- Investigators Brochure
- Submissions
- Communication
- Medical Science
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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