Core ICF Developer/Writer and Reviewer (Centralized role)
Fortrea(11 months ago)
About this role
A Clinical Informed Consent Specialist focused on the development and maintenance of Master Informed Consent Forms for clinical trials, ensuring alignment with study protocols and regulatory frameworks. The role emphasizes participant comprehension, regulatory compliance, and clear communication with study stakeholders.
Required Skills
- Informed Consent
- GCP Guidelines
- Regulatory Knowledge
- IND/NDA
- Medical Terminology
- Health Literacy
- Customer Service
- MS Word
- Written Communication
- Stakeholder Influence
+5 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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