Job Description
Join Mayo Clinic's world-class research team as a Clinical Research Coordinator and drive groundbreaking medical innovations. We're seeking a meticulous professional to manage complex clinical trials while ensuring regulatory compliance and participant safety. This pivotal role bridges cutting-edge science with compassionate patient care in our state-of-the-art facilities.
Responsibilities
- Oversee end-to-end clinical trial execution from protocol development to final reporting
- Ensure strict adherence to FDA regulations, ICH-GCP guidelines, and IRB protocols
- Recruit, screen, and enroll eligible research participants with precision
- Manage comprehensive participant data using REDCap and EDC systems
- Coordinate multidisciplinary teams including physicians, nurses, and biostatisticians
- Conduct regular site monitoring audits and prepare regulatory documentation
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- Certified Clinical Research Professional (CCRP) certification required
- Minimum 3 years experience in clinical trial coordination
- Expertise in FDA regulations, ICH-GCP, and HIPAA compliance
- Proficiency with EDC systems (e.g., Medidata Rave, Oracle) and REDCap
- Exceptional organizational skills and attention to detail
- Strong written and verbal communication abilities