About this role
Role Overview
- Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required
- Perform site monitoring visits
- Work with sites to adapt, drive and track subject recruitment plan
- Administer protocol and related study training to assigned sites
- Evaluate the quality and integrity of study site practices
- Manage the progress of assigned studies
- Ensure copies/originals of site documents are available for filing
- Create and maintain appropriate documentation regarding site management
Requirements
- 2.5 years of clinical research coordination experience at site level
- Nursing or University Degree (US Bachelor Level or equivalent) in one of the life sciences
- Knowledge of electronic data capture preferred
Benefits
- Health and welfare benefits
- Incentive plans
- Bonuses