Job Description
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
Job Tags
Full time, Work at office,