Centralized Study Analyst

Fortrea


Job Location:

Sofia - Bulgaria

Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Key Responsibilities

  • Manage clinical study systems (CTMS IWRS EDC) and user access.
  • Maintain study documentation including eTMF management and filing.
  • Act as a support to the Project Lead assisting with day-to-day study coordination and any ad hoc requests from the study teams.
  • 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

  • Minimum 2 years experience in clinical research.
  • Good knowledge of ICH-GCP and applicable regulatory requirements.
  • Strong organisational skills and attention to detail.
  • Effective communication and ability to work collaboratively.
  • Proficiency in MS Office and clinical systems/tools.

Learn more about our EEO & Accommodations request here.


Required Experience:

IC

Key ResponsibilitiesManage clinical study systems (CTMS IWRS EDC) and user access.Maintain study documentation including eTMF management and filing.Act as a support to the Project Lead assisting with day-to-day study coordination and any ad hoc requests from the study teams.Support data review activ...

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