Core ICF Developer/Writer and Reviewer (Centralized role)
Fortrea(11 months ago)
About this role
A clinical documentation specialist focused on informed consent forms and related clinical trial documents, ensuring they are accurate, compliant, and understandable for research participants. The role sits within clinical research to align consent content with study protocols, client requirements, and applicable regulatory frameworks. It also supports development of master templates and training materials to maintain document quality and consistency.
Required Skills
- Clinical Writing
- ICF Development
- Regulatory Knowledge
- GCP
- IND/NDA
- Medical Terminology
- Health Literacy
- Stakeholder Management
- Training Development
- MS Word
+3 more
Qualifications
- University/College Degree (Medical Preferred)
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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