Job Description
Join Mayo Clinic's world-class research team as a Clinical Research Coordinator, where you'll drive innovation in medical breakthroughs. This pivotal role bridges cutting-edge science with patient care in a collaborative environment. You'll manage complex clinical trials, ensure regulatory compliance, and contribute to life-changing research while working alongside leading physicians and scientists.
Responsibilities
- Design and implement clinical trial protocols in accordance with FDA/ICH guidelines
- Recruit, screen, and enroll study participants while maintaining ethical standards
- Monitor trial progress, collect accurate data, and maintain electronic case report forms
- Coordinate with multidisciplinary teams including physicians, nurses, and biostatisticians
- Ensure GCP compliance and prepare regulatory submissions for IRB approval
- Analyze trial data and prepare comprehensive reports for stakeholders
- Maintain meticulous documentation and audit trail for all study activities
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in GCP environment
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave, Oracle Clinical)
- Demonstrated knowledge of FDA regulations and clinical trial methodologies
- Exceptional organizational skills with attention to detail in documentation
- Strong communication abilities for patient interactions and team collaboration
- Experience with oncology or cardiovascular trials highly desirable