Piper Companies
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
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