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Centralized Study Analyst
Job Location:
Monthly Salary:
Posted:
3 July 2026 (30+ days ago)
Posted:
Application Deadline:
30 September 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
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
