Job Description
Join Mayo Clinic's prestigious research division as a Clinical Research Coordinator and drive breakthroughs in patient care. We're seeking a detail-oriented professional to manage complex clinical trials across oncology and cardiology departments. This role offers unparalleled mentorship, cutting-edge resources, and the opportunity to contribute to life-changing medical advancements while working alongside world-renowned physicians in Rochester's thriving medical ecosystem.
Responsibilities
- Oversee end-to-end clinical trial operations including protocol adherence, patient recruitment, and regulatory compliance
- Manage electronic data capture systems and ensure accurate documentation per FDA/ICH-GCP standards
- Coordinate multi-disciplinary research teams and maintain collaborative relationships with sponsors
- Monitor adverse events and implement safety protocols per institutional guidelines
- Analyze trial data and prepare comprehensive reports for regulatory submissions
- Mentor junior research staff and ensure continuous process improvement
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience in FDA-regulated trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in electronic data capture systems (e.g., Medidata Rave, Oracle Inform)
- Proven track record in oncology/cardiology trial management
- Strong knowledge of 21 CFR Part 11 and ICH-GCP guidelines
- Exceptional organizational skills and attention to regulatory documentation