Clinical Research Coordinator A

Job Description Summary

The Division of Gastroenterology Research Team is seeking a dedicated and professional Clinical Research Coordinator (CRC) to play a vital role in advancing our clinical trials program. As an essential member of our research team, the CRC will be instrumental in coordinating clinical trials and collecting and processing specimens across our clinical trials. This full-time position encompasses a range of responsibilities including the recruitment, scheduling, and retention of participants in retrospective/prospective observational data collection projects, investigator-initiated studies, and bio-specimen collection studies. Reporting directly to the Research Nurse Manager and working closely with Physician Investigators (PIs), the CRC will manage all facets of clinical trial coordination. This includes meticulous subject recruitment, detailed data entry, coordinating subject visits and follow-ups, as well as managing regulatory documentation.

Job Responsibilities

• Operational Execution: Managing day-to-day study activities, including subject recruitment, screening, enrollment, and conducting study visits.
• Regulatory Compliance: Preparing and maintaining essential study documentation such as protocols, informed consent forms, and IRB submissions to ensure adherence to federal and institutional guidelines.
• Data Management: Overseeing the construction of databases and case report forms (CRFs), as well as performing data entry, cleaning, and quality control for interim analyses.
• Coordination: Serving as a primary liaison between investigators, internal study teams, and external collaborators to track project milestones and timelines.
• Supervision: While typically working under moderate supervision, they may provide limited guidance/training orientation or task coordination to research coordinator.

Position Contingent Upon Funding