Certified Research Coordinator

Description

Position Summary

The Certified Research Coordinator (CRC) supports the successful execution of clinical and scientific research studies in accordance with federal regulations, institutional policies, and Good Clinical Practice (GCP) guidelines. This role ensures participant safety, data integrity, and regulatory compliance across all stages of research.

Key Responsibilities

• Coordinate day-to-day operations of assigned clinical trials and research protocols.
• Screen, recruit, consent, and schedule study participants according to protocol criteria.
• Collect, document, and manage study data in electronic case report forms (eCRFs).
• Ensure compliance with IRB, FDA, and sponsor requirements; maintain all regulatory documents.
• Monitor for adverse events, deviations, and ensure timely reporting.
• Serve as a liaison among investigators, sponsors, monitors, and participants.
• Prepare for audits, site monitoring visits, and inspections.
• Educate participants and site staff on study procedures and expectations.
  
  

Qualifications

• Bachelor's degree in healthcare, science, or related field (required).
• Certified Clinical Research Coordinator (CCRC or CCRP) through ACRP or SOCRA (required).
• 2 years of clinical research experience (preferred).
• Strong understanding of GCP, FDA regulations, HIPAA, and clinical trial processes.
• Proficient in Microsoft Office and research data platforms (e.g., REDCap, CTMS, EDC).
• Exceptional attention to detail, organization, and communication skills.
  
  

Work Environment

• Fast-paced, collaborative research setting.
• May involve extended screen time, patient interaction, and occasional travel for training or site visits.