ICF Reviewer II
Bucharestremote
Posted today · via Workday
About this role
Job Overview: Document Review Specialist I is responsible for reviewing Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP, FDA and other regional guidance. Document Review Specialist I may responsible for reviewing revised protocols and core ICF’s. Summary of Responsibilities: Review Country/Site Informed Consent Form to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines. Review Patient Recruiting materials (Advertisements) to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: gcp, teams
2
Level fit
We check your title trajectory against the seniority signal of the role.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is remote-eligible — we factor in your stated location and time-zone overlap.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
gcpteams
More at Fortrea
- View →Clinical Research Associate II YorkshireLeeds
- View →Site Start-up Specialist - FSPRemote Sweden
- View →Document Specialist II (seeking immediate joiners or with notice period less than 30 days)Bangalore
- View →Director, Talent Acquisition North AmericaDurham
- View →Safety Science Coordinator - IIBangalore
- View →Senior CRA - Sponsor DedicatedPrague