Clinical Research Coordinator

Piper Companies is seeking a highly organized and proactive Clinical Research Coordinator (CRC) to support clinical trials across multiple therapeutic areas on-site in the Newport Beach, CA area. This role is essential in ensuring smooth trial execution within a clinical site network, with a focus on phlebotomy and patient coordination.Key Responsibilities of the Clinical Research Coordinator:Oversee day-to-day clinical trial activities while ensuring compliance with GCP, IRB, and study protocolsConduct phlebotomy procedures and process biological specimens per protocolSchedule and lead study visits, including informed consent, data collection, and follow-upsMaintain accurate documentation in source records and electronic data capture (EDC) systemsCollaborate with sponsors, CROs, and site teams to uphold protocol adherence and data integrityAssist with regulatory submissions, monitoring visits, and audit preparationSupport subject recruitment, screening, and retention strategiesQualifications of the Clinical Research Coordinator: Bachelor's degree in a health-related field or equivalent experience2-4 years of experience in a clinical site network as a CRC or similar roleCertified or trained in phlebotomy, with proven venipuncture skillsStrong knowledge of ICH-GCP, FDA regulations, and clinical trial operationsProficient in EDC systems, CTMS, and Microsoft Office SuiteExceptional communication, organizational, and multitasking skillsCompensation and Benefits: Salary: $65,000-$70,000Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave, and Paid Holidays This job opens for applications on 8/15. Applications for this job will be accepted for at least 30 days from the posting date. #LI-KI1 #LI-ONSITEKeywords: Clinical research coordinator, clinical trials, GCP (Good Clinical Practice), IRB compliance, protocol adherence, FDA regulations, phlebotomy, venipuncture, biological specimen processing, Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), regulatory submissions, data collection, site network coordination, sponsor and CRO collaboration, subject recruitment, patient follow-up, audit preparation, quality assurance