Core ICF Developer/Writer and Reviewer (Centralized role)
Fortrea(11 months ago)
About this role
This role focuses on developing, reviewing, finalizing, and maintaining informed consent forms and other clinical trial documents to ensure they align with protocols and regulatory requirements. The position requires ensuring documents are clear, compliant with GCP and privacy regulations, and tailored to client-specific guidance. The role also supports template development, stakeholder communication, and training materials related to consent documentation.
Required Skills
- Informed Consent
- GCP
- Regulatory Compliance
- IND/NDA
- GDPR
- Medical Terminology
- Health Literacy
- Customer Service
- MS Word
- Communication
+7 more
Qualifications
- University 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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