Clinical Research Coordinator

Job Summary

Overseeing and coordinating all aspects of clinical trials, the full-time Clinical Research Coordinator will ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines while managing patient interactions and data management in a hybrid on-site environment.

Key responsibilities

• Coordinate patient recruitment, screening, and enrollment for clinical trials while maintaining study documentation and ensuring compliance with protocols
• Serve as the primary point of contact for participants, providing information about study protocols and monitoring patient progress throughout the study
• Ensure adherence to regulatory requirements by preparing and submitting necessary documentation and conducting training for study staff

Required qualifications

• Bachelor's degree in a related field; CCRC Certification and/or Master's degree preferred
• 3+ years of experience in clinical research, with 2+ years in independent trial management preferred
• Solid understanding of drug development processes, FDA, and ICH GCP guidelines
• Proficiency in using multiple software systems, with preference for experience with Florence, Advarra, and Greenphire
• Certifications in GCP, BLS, IATA, and CSSR (or willingness to acquire if hired)