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 Raleigh, NC 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 protocols
• Conduct phlebotomy procedures and process biological specimens per protocol
• Schedule and lead study visits, including informed consent, data collection, and follow-ups
• Maintain accurate documentation in source records and electronic data capture (EDC) systems
• Collaborate with sponsors, CROs, and site teams to uphold protocol adherence and data integrity
• Assist with regulatory submissions, monitoring visits, and audit preparation
• Support subject recruitment, screening, and retention strategies

Qualifications of the Clinical Research Coordinator:

• Bachelor's degree in a health-related field or equivalent experience
• 2–4 years of experience in a clinical site network as a CRC or similar role
• Certified or trained in phlebotomy, with proven venipuncture skills
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial operations
• Proficient in EDC systems, CTMS, and Microsoft Office Suite
• Exceptional communication, organizational, and multitasking skills

Compensation and Benefits:

• Salary: $55,000-$70,000
• Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave, and Paid Holidays

This job opens for applications on 6/9. Applications for this job will be accepted for at least 30 days from the posting date.

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Keywords: 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.