Senior Clinical Research Associate - FS

Role: Senior Clinical Research Associate supporting clinical trial execution within an FSP team, primarily conducting onsite monitoring activities. Responsibilities: perform source verification against source documents, ensure protocol compliance, manage study documentation and investigator site files, address data discrepancies, and oversee regulatory documentation and site budgets. Requirements: Bachelor's degree in a clinical or health-related field; 5-7 years of independent onsite monitoring experience, preferably with Schedule 1 knowledge; strong organizational skills, ability to manage multiple projects, and knowledge of ICH/GCP and country-specific regulations. HighValue: experience with Schedule 1, extensive site management, and monitoring in clinical research. WorkSetup: up to 70-85% travel.