Perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with contracted scope of work and regulatory requirements
Job Summary
Perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with contracted scope of work and regulatory requirements.
Administer protocol and related study training to assigned sites and establish regular lines of communication to manage ongoing project expectations and issues.
Act as a mentor for clinical staff, including conducting co-monitoring and training visits, and collaborate with study team members for project execution support.
Matching Summary
Perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with contracted scope of work and regulatory requirements.
Salary
Base: $102,500.00 - $170,900.00; Bonus/Equity: Not specified; Benefits: Health and wellness benefits offered
Skills & Requirements
Must-have
Site monitoring visits
Subject recruitment plan
Protocol and study training
GCP and ICH guidelines
Clinical trial documentation
Nice-to-have
Mentoring clinical staff
Financial management of site
Effective time management
Building effective relationships
Key Requirements
At least 3 years of on-site monitoring experience
Bachelor's Degree in scientific or healthcare discipline preferred