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.

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

• 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