Job Description
Join Mayo Clinic's prestigious Cardiovascular Research Division as we pioneer breakthrough treatments for heart disease. This pivotal role leads multi-center clinical trials from protocol development to FDA submission, collaborating with Nobel laureates and industry partners. Our state-of-the-art facilities offer unparalleled resources for translational research, while our integrated care model ensures your work directly impacts patient outcomes.
Benefits include comprehensive health coverage, 401(k) matching, and $10,000 annual professional development fund. Mayo Clinic consistently ranks among Fortune's '100 Best Companies to Work For'.
Responsibilities
- Design and execute Phase II-III cardiovascular clinical trials across 15+ sites
- Manage complex budgets exceeding $2M with 98% audit compliance
- Lead FDA submissions and regulatory interactions (IND/IDE)
- Mentor 3+ junior coordinators using standardized training protocols
- Develop innovative eCRF systems reducing data entry errors by 40%
- Present findings at major conferences (ACC, AHA, ESC)
Qualifications
- Master's degree in Clinical Research or related field with 5+ years' trial coordination
- Certified Clinical Research Professional (CCRP) or equivalent
- Proven experience with cardiac device or drug trials (IDE/IND)
- Advanced proficiency in REDCap and Medidata Rave
- Strong FDA audit history with zero major findings
- Published author in peer-reviewed cardiology journals