Core ICF Developer/Writer and Reviewer (Centralized role)
Fortrea(11 months ago)
About this role
A Senior Informed Consent Specialist responsible for authoritative oversight of informed consent forms and related clinical trial documentation. The role ensures documents are clear, participant-friendly, and aligned with protocols and applicable regulatory frameworks. The position supports study start-up through development of master templates and stakeholder collaboration to maintain document quality and compliance.
Required Skills
- Informed Consent
- Clinical Documents
- Drug Development
- Regulatory Knowledge
- GCP
- GDPR
- Medical Terminology
- MS Word
- Written Communication
- Stakeholder Management
+3 more
Qualifications
- University Degree
- Medical Degree (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.
View more jobs at Fortrea →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Fortrea
Similar Jobs
Informed Consent Writer
Clinical Careers Page(1 month ago)
Informed Consent Writer
Clinical Careers Page(24 days ago)
ICF Manager
Clinical Careers Page(1 month ago)
Informed Consent Writer
Clinical Careers Page(1 month ago)
Internship - Clinical Affairs AI
Haemonetics(1 month ago)
Site Research Assistant - West Jordan, UT
IQVIA(2 months ago)