Job Description
Join Mayo Clinic's elite research team as a Clinical Research Coordinator where innovation meets patient care. You'll orchestrate groundbreaking clinical trials in our state-of-the-art facilities, collaborating with world-renowned physicians to advance medical science. We offer competitive compensation, comprehensive benefits, and unparalleled professional development opportunities in an environment that prioritizes both scientific excellence and patient-centered values.
Responsibilities
- Design and implement comprehensive clinical trial protocols ensuring FDA compliance and institutional standards
- Recruit, screen, and enroll qualified participants while maintaining strict ethical guidelines
- Manage complex data collection processes using electronic health records and specialized software
- Coordinate multidisciplinary teams including physicians, nurses, and regulatory specialists
- Monitor adverse events and ensure timely reporting to regulatory bodies
- Prepare regulatory submissions and maintain meticulous trial documentation
Qualifications
- Master's degree in Clinical Research, Nursing, Life Sciences, or related field
- 3+ years of clinical research coordination experience in FDA-regulated trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in ICH-GCP guidelines and 21 CFR Part 11 compliance
- Advanced proficiency in clinical trial management systems (e.g., Medidata Rave)
- Exceptional organizational skills with ability to manage multiple complex protocols
- Strong written and verbal communication abilities for stakeholder interactions