Job Description
Join Mayo Clinic's prestigious research division as a Clinical Research Coordinator and drive breakthroughs in patient care. At the forefront of medical innovation, you'll manage pivotal clinical trials while collaborating with world-renowned physicians and scientists. Mayo offers unparalleled resources, cutting-edge facilities, and a culture where your expertise directly impacts global healthcare standards. Enjoy comprehensive benefits including competitive compensation, flexible scheduling, and robust professional development opportunities.
Responsibilities
- Design, implement, and oversee clinical trial protocols ensuring compliance with FDA regulations and GCP standards
- Recruit, screen, and enroll participants while maintaining accurate electronic health records
- Coordinate multi-disciplinary research teams and manage complex trial logistics
- Analyze and interpret clinical data using SAS/R programming and statistical methodologies
- Prepare regulatory submissions and maintain audit-ready documentation
- Monitor adverse events and ensure participant safety protocols are strictly followed
- Leverage REDCap and Epic systems for data management and reporting
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in a hospital or academic setting
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Expertise in FDA 21 CFR Part 820 and ICH-GCP guidelines
- Proficient in statistical software (SAS, R) and EDC systems
- Exceptional communication skills with ability to translate complex medical concepts
- Demonstrated project management experience with multi-million dollar budgets
- Valid Minnesota nursing license or willingness to obtain within 90 days