About this role
The Senior Regulatory Medical Writer role involves leading the authoring and development of high complexity clinical regulatory documents in a remote setting within the UK, Greece, Spain, or Portugal. The position requires coordinating with various teams to deliver key documents for clinical trials, primarily focusing on protocols and study reports.
Required Skills
- Regulatory Writing
- Clinical Documents
- CSRs
- Protocols
- Medical Data Interpretation
- Project Leadership
- Communication
- Team Coordination
- Regulatory Guidelines
- Biostatistics
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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