Clinical Research Coordinator(Regulatory)

Overview
Join our dynamic clinical research team as a Clinical Research Coordinator (Regulatory), where your expertise will drive the success of groundbreaking clinical trials. This vital role involves managing regulatory documentation, ensuring compliance with industry standards, and supporting the integrity of research processes.

Skills:

3+ years of experience in clinical research supporting regulatory compliance and study documentation.

Skilled in managing and tracking regulatory documents including IRB correspondence, FDA forms, CVs, medical licenses, and SAE submissions.

Strong knowledge of FDA GCP, GLP, and local IRB regulatory requirements

1+ year oncology clinical research experience

CCRP certification with working experience in Epic systems

Job Type: Temporary

Pay: $67.00 per hour

Expected hours: 40 per week

Work Location: In person