Senior Clinical Research Coordinator

Primary Responsibilities

• Lead study management
• Mentor junior staff
• Ensure compliance with regulatory standards
• Maintain participant safety

Skills & Requirements

• Associate degree required; Bachelor's degree preferred
• Hands-on experience as a Clinical Research Coordinator in a research site, hospital, or private practice setting
• Proficiency in clinical trial management systems (CTMS) and EDC systems
• Strong knowledge of clinical research regulations, FDA guidelines, and ICH-GCP standards
• Phlebotomy skills and/or certification preferred
• Excellent organizational, leadership, and critical thinking abilities
• Strong verbal and written communication skills
• Detail-oriented with a commitment to data accuracy, patient safety, and regulatory compliance

The Senior Clinical Research Coordinator's Responsibilities Will Be

• Manage clinical trials from initiation to close-out, including high-complexity and high-enrollment studies
• Supervise and mentor junior Clinical Research Coordinators, providing guidance and training
• Recruit, screen, and consent study participants in accordance with study protocols
• Dispense investigational products and monitor participant adherence to study requirements
• Collect and process biological specimens, perform vital signs assessments, ECGs, and phlebotomy
• Schedule and conduct participant visits and assessments as outlined in the protocol
• Accurately document and enter data into electronic data capture (EDC) systems, resolving queries as needed
• Maintain regulatory binders and ensure readiness for monitoring visits
• Track and report adverse events, ensuring timely submission of serious adverse event (SAE) reports
• Act as a liaison between sponsors, monitors, and referring physicians

Pay

$30 to $38 per hour

Contact Information

If you are having difficulty in applying or if you have any questions, please contact Alex Kelly at a.kelly@proclinical.com

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