Clinical Trial Liaison

Bachelor’s degree in healthcare related field
Minimum of 3 years of experience in clinical research, with a focus on site management and patient recruitment
Strong knowledge of clinical trial protocols, GCP guidelines, and regulatory requirements
Proven ability to work independently and manage multiple clinical sites simultaneously
Excellent communication, organizational, and problem-solving skills
Ability to build strong relationships with site staff and foster a collaborative working environment
Flexibility to travel as required for site visits and meetings

Serve as the primary liaison between the clinical trial sponsor and participating sites, ensuring effective communication and collaboration
Support clinical sites in meeting patient recruitment goals by providing guidance on strategies, tools, and resources
Monitor site performance and provide proactive support to resolve any issues related to protocol compliance, patient recruitment, and data collection
Ensure that all site staff are trained and compliant with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements
Collaborate with site staff to identify and overcome barriers to patient recruitment and retention
Track site progress and prepare reports on site performance, recruitment metrics, and study milestones
Conduct regular site visits, both remote and in-person, to provide hands-on support and address any operational challenges
Work closely with cross-functional teams, including project management, regulatory affairs, and data management, to ensure seamless study execution
Maintain a thorough understanding of cardiovascular disease, study protocols, and the specific needs of the patient population