Fortrea
ICF Reviewer I
Sofia
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hirly's read of this role
- Seniority
- Mid level
- Country
- BG
- Work mode
- On-site / unstated
- First seen by hirly
- 3 Oct 2026
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the posting
Summary of Responsibilities:
Review and implementation of relevant study-specific plans that describe the required expectations for assigned tasks
Support system compliance and system data entry, as applicable
File required task-related documentation in the Electronic Trial Master File (eTMF)
Review initial/amended Country/Site ICFs in compliance with Sponsor requirements, local regulatory requirements and Good Clinical Practice (GCP) guidelines.
Liaising and follow-up with local teams, Start-up Project Managers, and Sponsors to assure timely approval of Informed Consent Forms in order to meet submission deadlines.
Qualifications (Minimum Required):
University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology)
Fortrea may consider relevant and equivalent experience in lieu of educational requirements
Experience (Minimum Required):
Working knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines.
2 years’ work experience in clinical research
Previous interaction with operational project teams preferred.
Preferred Qualifications Include:
Computer proficiency in MS Office (Word, Excel, PowerPoint, Access, Outlook e-mail and internet services)
Good written and oral communication skills
Well-developed organizational skills
Excellent proof-reading skills
Learn more about our EEO & Accommodations request here .
Listed on hirly, a job board. hirly is not the employer: Fortrea is hiring for this role.
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