Medix
The Clinical Research Site Manager is responsible for managing the day-to-day operations of a clinical trial site to ensure high-quality, compliant, and efficient execution of clinical studies. This role oversees site staff, coordinates with sponsors and CROs, ensures regulatory compliance, and supports patient recruitment and retention activities.
Key Responsibilities:
Manage site operations to ensure studies are conducted in compliance with protocols, GCP, and regulatory requirements
Supervise and support site personnel (e.g., study coordinators, nurses, and support staff)
Maintain essential regulatory documents and site files (ISF)
Act as primary liaison with sponsors, CROs, and monitors
Oversee and support patient recruitment, enrollment, and retention efforts
Ensure accurate and timely data entry and query resolution in EDC systems
Prepare for and support monitoring visits, audits, and inspections
Track study budgets, assist with contract execution, and manage site-related finances