Clinical Research Associate I (CRA I) – Italy Location: Italy Working arrangement: Home-based with travel to clinical trial sites Employment type: Full-time, permanent The Opportunity We are partnering with an international clinical research organisation seeking a
Specific activities and responsibilities: Plan, coordinate, and execute Computerized System and SW applications Validation (CSV) activities for client projects in compliance with GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11 requirements. Prepare,