Job Description
Join Mayo Clinic's prestigious research team as a Clinical Research Coordinator and shape the future of healthcare innovation. We seek a meticulous professional to manage complex clinical trials while ensuring regulatory compliance and patient safety. This role offers unparalleled opportunities to collaborate with world-renowned physicians and contribute to groundbreaking medical advancements.
At Mayo Clinic, you'll work in a state-of-the-art facility with cutting-edge technology and comprehensive benefits. Our patient-centered approach ensures your work directly impacts global healthcare outcomes while advancing your career in a supportive environment.
Responsibilities
- Oversee all aspects of clinical trial protocols including patient recruitment, enrollment, and data collection
- Ensure strict adherence to FDA regulations, GCP standards, and institutional policies
- Coordinate interdisciplinary research teams and maintain comprehensive trial documentation
- Monitor adverse events and ensure timely reporting to regulatory bodies
- Develop and maintain patient education materials and consent forms
- Analyze trial data and prepare regulatory submissions and progress 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 Professional (CCRP) or equivalent certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave, Veeva Vault)
- Exceptional attention to detail with strong organizational skills
- Excellent written and verbal communication abilities
- Experience with IRB submissions and protocol development