
Site Management Specialist
2 days ago
Job Overview
The successful candidate will be responsible for managing clinical trial sites in accordance with good clinical practice (GCP) guidelines. This will involve performing site monitoring visits, working closely with sites to adapt and drive subject recruitment plans, and administering protocol training to assigned sites.
Main Tasks and Responsibilities
- Ensure compliance with study protocols and regulatory requirements through site monitoring visits.
- Support sites in adapting and driving subject recruitment plans to meet project needs.
- Establish regular lines of communication with sites to manage ongoing project expectations.
- Evaluate site practices related to the proper conduct of protocols and adherence to regulations.
Qualifications
- Bachelor's degree in a scientific discipline or healthcare field.
- Equivalent combination of education, training, and experience may be accepted in lieu of degree.
- Basic knowledge of GCP guidelines and ability to apply them.
- Good therapeutic and protocol knowledge as provided in company training.
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