Develop and maintain strong relationships with key personnel at clinical trial sites, including principal investigators, site coordinators, and other site staff
Serve as a bridge between the sponsor and clinical trial sites, ensuring clear and timely communication of study protocols, updates, and key information
Conduct Monitoring Oversight Visits and regular site engagement activities to ensure high-quality trial execution
Design customized site-level engagement plans to help drive enrollment and support timely patient recruitment
Collaborate with CRO CRAs and Medical Science Liaisons to identify, mitigate and resolve site-level challenges
Participate in feasibility and site qualification visits, collaborating with CRO representatives
Represent the sponsor at local and regional patient advocacy or support group meetings when needed
Track and report site engagement activities, enrollment status, and performance metrics
Requirements
Bachelor's degree in a relevant field (life sciences, nursing, healthcare management)
Proven experience in clinical research and site relationship management
Excellent communication and interpersonal skills
Proactive problem-solving abilities
Strong organizational and project management skills
Solid understanding of GCP and regulatory requirements
Must reside within 30-45 minutes of one of the following airports: Dallas (DFW), Houston (IAH), Chicago (ORD), Minneapolis (MSP), or Detroit (DTW)