Clinical Trial Liaison

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Requirements:

• Bachelor’s degree in healthcare related field.
• Minimum of 3 years of experience in clinical research.
• Experience with site management and patient recruitment.
• Desirable experience in cardiovascular and/or imaging clinical trials.
• Strong knowledge of clinical trial protocols, GCP guidelines, and regulatory requirements.
• Proven ability to work independently and manage multiple clinical sites.
• Excellent communication, organizational, and problem-solving skills.
• Flexibility to travel up to 50% for site visits and meetings.

Responsibilities:

• Serve as the primary liaison between the clinical trial sponsor and participating sites.
• Support clinical sites in meeting patient recruitment goals.
• Monitor site performance and provide proactive support to resolve issues.
• Ensure site staff are trained and compliant with study protocols and regulations.
• Collaborate with site staff to identify barriers to recruitment and retention.
• Track site progress and prepare reports on performance and recruitment metrics.
• Conduct regular site visits to provide support and address operational challenges.
• Work closely with cross-functional teams to ensure seamless study execution.