Clinical Research Coordinator at Insight Global Santa Maria, CA

Job Description

Qualifications

• •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
• •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

Benefits

Responsibilities

• •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