Description
We are seeking experienced candidates to perform monitoring and site management work, ensuring sites conduct studies and report data according to protocols, regulations, and sponsor requirements.
The position requires 65-70% nationwide travel.
Essential Functions:
- Conduct site monitoring visits in accordance with contracted scope of work and regulatory requirements
- Collaborate with sites to adapt and drive subject recruitment plans
- Provide protocol and study training to assigned sites and establish communication channels
- Evaluate study site practices and escalate quality issues as needed
- Manage study progress, track regulatory submissions, and resolve data queries
- Maintain accurate documentation and ensure compliance with GCP and ICH guidelines
Minimum Recruitment Standards:
- 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
The potential base pay range for this role is $64,000.00 - $189,000.00 per year.