Job Description
Join Mayo Clinic's pioneering clinical research team where innovation meets compassionate care. As a Clinical Research Coordinator, you'll drive groundbreaking studies that shape the future of medicine in our state-of-the-art facilities. Enjoy competitive benefits, professional development opportunities, and the chance to contribute to life-changing discoveries.
Responsibilities
- Manage complex clinical trials from protocol development to closeout
- Recruit and screen participants ensuring strict protocol compliance
- Collect, analyze, and report clinical data with precision
- Coordinate multidisciplinary research teams and vendor relationships
- Ensure regulatory compliance (FDA, GCP, HIPAA) documentation
- Monitor patient safety and adverse event reporting protocols
- Present research findings at national conferences and publications
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 3+ years clinical trial coordination experience
- Certified Clinical Research Professional (CCRP) preferred
- Expertise in electronic data capture systems (e.g., REDCap)
- Strong knowledge of FDA regulations and GCP standards
- Exceptional communication and stakeholder management skills
- Proven experience with IRB submissions and compliance
- Ability to manage competing priorities in fast-paced environments