Job Description
Join Mayo Clinic's pioneering research division as a Clinical Research Coordinator and shape the future of healthcare innovation. We're seeking a detail-oriented professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. Work alongside world-renowned physicians in a state-of-the-art facility where your contributions directly impact medical breakthroughs.
Mayo Clinic offers unparalleled professional development, comprehensive benefits, and a collaborative environment committed to excellence. If you're passionate about advancing medical science through rigorous research protocols, this is your opportunity to thrive.
Responsibilities
- Coordinate and execute multi-phase clinical trials from protocol development to final reporting
- Recruit, screen, and enroll eligible participants while maintaining strict confidentiality
- Monitor trial progress, collect data, and ensure adherence to FDA/ICH-GCP standards
- Prepare regulatory submissions and maintain accurate study documentation
- Liaise with sponsors, IRBs, and multidisciplinary healthcare teams
- Analyze trial data and prepare comprehensive study reports
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience with FDA-regulated trials
- Certified Clinical Research Coordinator (CCRC) or equivalent certification
- Expertise in regulatory compliance (FDA, EMA, ICH-GCP)
- Advanced proficiency in EDC systems (e.g., Medidata Rave)
- Exceptional organizational and communication skills
- Experience with oncology or immunology trials highly desirable