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Posted 8 hours ago

Centralized Study Analyst

at Fortrea

Sofia, BulgariaOn-site
GCP

Responsibilities

  • Maintain study documentation, including eTMF management and filing.
  • Support data review activities and follow up with CRAs on outstanding issues.
  • Generate study reports and track study metrics as required.
  • Coordinate internal and external communications across study teams.
  • Support study operations, including payments (sites/vendors), system setup, and compliance tracking.

Requirements

  • Good knowledge of ICH-GCP and applicable regulatory requirements.
  • Effective communication and ability to work collaboratively.
  • Proficiency in MS Office and clinical systems/tools.

Experience

  • Requirements Minimum 2 years’ experience in clinical research.

Additional details

  • Responsibilities Manage clinical study systems (CTMS, IWRS, EDC) and user access.
  • Act as a support to the Project Lead, assisting with day-to-day study coordination and any ad hoc requests from the study teams.
  • Strong organisational skills and attention to detail.
  • Learn more about our EEO & Accommodations request here .

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