About this role
Role Overview
- serve as primary contact between Sponsor and Investigational Site
- ensure compliance with clinical trial protocols and regulations
- assist with site selection and qualification
- monitor site activities and ensure timely resolution of issues
- contribute to process improvement and mentor other Site Managers
Requirements
- 3-5 years of experience in site management
- knowledge of clinical trial protocols and guidelines
- ability to operate independently with limited supervision
Benefits
- inclusive work environment
- diversity and dignity of employees