Clinical Research Coordinator

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

Job summary

Piper Companies is seeking a Clinical Research Coordinator (CRC) for a full-time, onsite position in Raleigh, NC. The CRC will play a vital role in overseeing clinical trials, collaborating with various stakeholders while ensuring compliance and maintaining documentation. Applicants should have at least 2 years of clinical research experience, strong phlebotomy skills, and excellent leadership abilities.

Benefits

Medical benefits

Dental benefits

Vision benefits

401K plan

Sick leave if required by law

Qualifications

• Minimum of 2 years as a clinical research coordinator.
• Strong knowledge of research protocols and ethical standards.
• Ability to manage teams and handle multiple responsibilities.

Responsibilities

• Support study investigators in participant screening and data entry.
• Maintain case report forms and ensure compliance with protocols.
• Oversee and mentor clinical research staff.

Skills

Phlebotomy

Regulatory compliance

Leadership

Communication

Organizational skills

Education

Bachelor's degree

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 Clinical Research Coordinator (CRC) to join a a trusted leader advancing the future of medicine for a full-time, onsite position located in Raleigh, NC. The Clinical Research Coordinator (CRC) will collaborate with the Principal Investigator (PI), sponsors, and clinical trial site management to oversee, support, and ensure compliance in all aspects of daily clinical trial activities, playing a vital role in the study's successful conduct.

Responsibilities of the Clinical Research Coordinator (CRC) include:

• Support study investigators in participant screening, eligibility review, and data collection/entry.
• Maintain and organize case report forms, documentation, and adherence to research protocols and compliance standards.
• Provide oversight, mentorship, and training for clinical research staff, including assisting with hiring and onboarding.
• Contribute to study start-up, maintenance, and close-out activities, demonstrating flexibility with assignments.
  
  

Qualifications for the Clinical Research Coordinator (CRC) include:

• Minimum of 2 years as a clinical research coordinator at a clinical site.
• Strong knowledge and experience with phlebotomy.
• Strong knowledge of research protocols, regulatory compliance, and ethical standards.
• Excellent organizational, communication, and leadership skills to manage teams and processes effectively.
• Ability to handle multiple responsibilities flexibly while maintaining attention to detail in all tasks.
• Bachelor's degree preferred.
  
  

Compensation for the Clinical Research Coordinator (CRC):

• Salary Range: $55,000-$70,000 /year
• Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K
  
  

This job opens for applications on 6/9. Applications for this job will be accepted for at least 30 days from the posting date.

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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