A Site Manager is responsible for overseeing and managing the operations of a specific site, which can vary based on the industry. Their duties revolve around ensuring that work is performed efficiently, safely, and according to the established schedule and budget. Here’s a breakdown of what a site manager typically does across different industries:
- Site Operations: Oversee the day-to-day management of clinical trials at the research site, ensuring all activities adhere to the study protocol.
- Staff Supervision: Coordinate with Clinical Research Coordinators, Principal Investigators, and other medical staff involved in the study.
- Regulatory Compliance: Ensure the site complies with all regulatory requirements, including Good Clinical Practice (GCP), ethics guidelines, and study-specific requirements.
- Patient Management: Oversee the recruitment, enrollment, and care of participants in clinical trials.
- Data Quality: Ensure accurate and timely collection and reporting of study data, including managing case report forms (CRFs).
