Centralized Study Analyst

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 ourEEO & Accommodations request here.