Clinical Research Coordinator

The Clinical Research Coordinator (CRC) collaborates with investigators, research teams, clinical departments, IRBs, and sponsors to plan, implement, and manage clinical trials and research projects. Responsibilities include participant recruitment, screening, enrollment, conducting protocol-required visits, data collection, and coordinating sponsor monitoring or federal audits. The CRC ensures compliance with federal and state regulations, institutional policies, and maintains accurate documentation, adverse event reporting, and study drug accountability.

Must Haves:

• Bachelors in a science or related field. A combination of education and/or additional job-related experience in lieu of the degree.
• 2-3 years of experience conducting clinical trials required; worked as primary research coordinator for at least 5 drug or device trials.
• 2-3 years of experience interacting with patients in a healthcare setting
• Experience using electronic data capture software and Clinical Trial Management Systems
• BLS cert
• Oncology experience

Plusses:

• Certified Clinical Research Professional (CCRP), within 12 - months or
• Certified Clinical Research Coordinator ACRP (CCRC-ACRP) within 12 - months or
• Certified Clinical Rearch Coordinator SCRA (CCRC-SCRA) within 12 - months or
• Certified Phlebotomy Technician (ANCC)
• Certified Clinical Research Professional (CCRP), within 12 - months or