Clinical Research Coordinator

Piper Companies; Raleigh (NC); On-site; USD 55,000 - 70,000; Full time

Job summary

Piper Companies is looking for a detail-oriented Clinical Research Coordinator to enhance its clinical research team in Raleigh, NC. This key role supports clinical trials by managing various activities from document maintenance to patient recruitment, requiring strong phlebotomy skills and extensive knowledge of regulatory standards. Candidates should have a health-related degree and relevant experience in a clinical setting, along with exceptional multitasking and organizational abilities.

Benefits

Comprehensive Benefits: Medical, Dental, Vision

401K and PTO

Sick Leave as required by law

Holidays

Qualifications

• 2–4 years of experience as a CRC or similar role.
• Certified in phlebotomy with proven venipuncture skills.
• Strong knowledge of ICH-GCP and FDA regulations.

Responsibilities

• Coordinate day-to-day clinical trial activities in compliance with GCP.
• Schedule and conduct study visits including informed consent.
• Maintain documentation in source documents and EDC systems.

Skills

Phlebotomy

Communication

Organizational skills

Multitasking

Education

Bachelor’s degree in health-related field

Tools

EDC systems

CTMS

Microsoft Office Suite

Job description

Join to apply for the Clinical Research Coordinator role at Piper Companies

Join to apply for the Clinical Research Coordinator role at 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

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Business Consulting and Services

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