What are the responsibilities and job description for the Clinical Research Quality Regulatory Coordinator position at BVL Clinical Research?
BVL Clinical Research is seeking a Clinical Research Quality Regulatory Coordinator for a full-time position at their Kansas City, Missouri, United States location.
In this role, the Coordinator will ensure compliance with regulations, sponsor requirements, and internal quality standards for all clinical trial activities at the private site. Key responsibilities include managing regulatory documents, overseeing quality, and maintaining inspection readiness to uphold high standards in clinical trial execution across various studies.
Requirements:
- Bachelor's degree in life sciences, healthcare, or a related field
- 2 years of experience in clinical research, preferably at a private site or research clinic
- Proficiency in IRB submissions, regulatory binders, and clinical research SOPs
- Familiarity with FDA regulations, ICH-GCP guidelines, and sponsor expectations for private sites
- Proficient in Microsoft Office and eRegulatory systems
- 2-5 years of clinical research experience
- Location must be commutable to Kansas City, Missouri, United States