Clinical Research Coordinator

Piper Companies is seeking a detail-oriented and proactive Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have hands-on phlebotomy experience and a strong background working within a clinical site network environment. This role is essential in supporting the execution of clinical trials across multiple therapeutic areas.

Responsibilities for the Clinical Research Coordinator:

• Coordinate and manage day-to-day clinical trial activities in compliance with GCP, IRB, and protocol requirements
• Perform phlebotomy and process biological specimens per protocol
• Schedule and conduct study visits, including informed consent, data collection, and subject follow-up
• Maintain accurate and timely documentation in source documents and electronic data capture (EDC) systems
• Collaborate with sponsors, CROs, and site network teams to ensure protocol adherence and data integrity
• Assist with regulatory submissions, monitoring visits, and audit preparation
• Support subject recruitment, screening, and retention strategies

Qualifications for the Clinical Research Coordinator:

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

Compensation for the Clinical Research Coordinator:

• Salary Range: $55,000-$70,000
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays