Clinical Research Coordinator

Fully onsite - Direct Hire - ideally 2 years of CRC experience needed prior.

Job Title:

Clinical Research Coordinator (CRC)

The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical research studies. This role ensures studies are conducted in compliance with protocol requirements, Good Clinical Practice (GCP), institutional policies, and regulatory guidelines. The CRC works closely with investigators, study sponsors, research participants, and regulatory bodies to ensure the successful execution of clinical trials.

• Coordinate and manage clinical research studies from start-up through close-out
• Screen, recruit, and enroll study participants according to protocol criteria
• Obtain and document informed consent in accordance with regulatory requirements
• Schedule and conduct study visits, procedures, and follow-ups
• Collect, document, and maintain accurate study data in source documents and electronic data capture (EDC) systems
• Ensure compliance with study protocols, GCP, IRB requirements, and applicable regulations
• Prepare and maintain regulatory documents, including IRB submissions, amendments, and continuing reviews
• Serve as the primary point of contact for sponsors, monitors, and study participants
• Assist with monitoring visits, audits, and inspections
• Track and report adverse events and protocol deviations
• Maintain study supplies, investigational product accountability, and inventory
• Collaborate with investigators and research team members to ensure study timelines and goals are met

• 2 Years of CRC Experience
• Comfortable working in a small team setting in a fast paced environment