Centralized Study Spec I at Fortrea
Who can apply
The employer hasn’t stated batch, branch or CGPA requirements for this role. Upload your résumé to see how well you match.
About this role
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-u…
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