Clinical Research Coordinator

Piper Companies is seeking a Clinical Research Coordinator for a trusted partner in clinical development located in Raleigh, North Carolina (NC). The Clinical Research Coordinator will be responsible for coordinating and supporting clinical research activities by overseeing participant screening, data management, team mentorship, regulatory compliance, and study lifecycle operations. This position will sit on-site in Raleigh, NC.

Responsibilities of the Clinical Research Coordinator:

• Support clinical trials by screening participants, reviewing eligibility, and maintaining accurate case documentation.
• Oversee data integrity through timely data collection, entry, and management of case report forms and study records.
• Mentor and train junior research staff, providing guidance and oversight to ensure protocol compliance and quality standards.
• Ensure regulatory compliance by adhering to research protocols, laws, and institutional policies.
• Contribute to team operations by assisting with study start-up, maintenance, and close-out, and participating in hiring and onboarding processes.
• Adapt to dynamic needs by managing multiple study assignments and supporting cross-functional research initiatives.

Qualifications for the Clinical Research Coordinator:

• 2-3 years of clinical research coordination experience with strong knowledge of clinical trial protocols and regulatory guidelines (GCP, CFR, HIPAA).
• Phlebotomy experience is required, along with prior experience as a Medical Assistant, LPN, or RN.
• Detail-oriented and highly confidential, with a strong commitment to patient privacy and data integrity.
• Preferred certifications include GCP and Advanced CRC, with demonstrated leadership and interpersonal skills.

Compensation for the Clinical Research Coordinator:

• Salary Range : $60,000-$68,000/year
• Comprehensive Benefits : Sick leave if required by law, medical, dental, vision, 401K

This job opens for applications on 07/30/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Clinical Research, Clinical Research Coordinator, Clinical Operations Coordinator, Clinical Trial Coordinator, Clinical Project Coordinator, Clinical Trials, Research Coordinator, Participant Screening, Case Documentation, Data Integrity, Case Report Forms, Study Records, Staff Training, Protocol Compliance, Regulatory Compliance, GCP, CFR, HIPAA, Study Start-Up, Study Maintenance, Study Close-Out, Multi-Study Management, Cross-Functional Research, Phlebotomy, Medical Assistant, LPN, RN, Patient Privacy, Data Management, Advanced CRC, Leadership, Interpersonal Skills

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