Clinical Research Coordinator II

Piper Companies is seeking a Clinical Research Coordinator II (CRC) to join a trusted leader advancing the future of medicine for a full-time, onsite position located in Charleston, SC. The Clinical Research Coordinator II (CRC) will independently coordinate and manage multiple clinical trials, ensuring protocol compliance, participant safety, and successful recruitment while supporting site operations and mentoring junior staff.

Responsibilities of the Clinical Research Coordinator II (CRC) include:

• Coordinate and execute multiple clinical trials independently, ensuring adherence to study protocols and participant safety.
• Develop and implement recruitment strategies to meet or exceed enrollment goals, including phone screening and outreach.
• Perform study-related procedures such as phlebotomy, ECGs, pulmonary function testing, and other protocol-specific assessments.
• Maintain accurate and timely documentation in source documents, progress notes, and electronic data systems.
• Support site-level quality assurance and staff development through mentoring and peer review of study criteria.

Qualifications for the Clinical Research Coordinator II (CRC) include:

• Bachelor’s degree in a relevant field.
• Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar clinical research role.
• Strong attention to detail and ability to manage multiple studies simultaneously.
• Proficiency in clinical trial management systems and electronic data capture platforms.
• Demonstrated interest in clinical research and commitment to participant care and protocol compliance.

 Compensation for the Clinical Research Coordinator II (CRC):

• Salary Range: $60,000-$65,000 /year
• Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 9/5/25. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Clinical Research Coordinator, CRC, Clinical Trials, Clinical Research, Study Coordinator, Phlebotomy, EDC, Case Report Forms, Patient Recruitment, Protocol Compliance, Source Documentation, Adverse Event Reporting, Investigator Meetings, Clinical Data Collection, Clinical Site Operations, Clinical Trial Management System, Pulmonary Function Testing, ECG, Holter Monitoring, IRB Reporting, Study Medication Dispensing, Quality Assurance, Mentoring, Healthcare Research

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