Job Description
Join Mayo Clinic's prestigious clinical research division where innovation meets compassionate care. As a Clinical Research Coordinator, you'll drive groundbreaking medical advancements while ensuring protocol integrity and patient safety. Our state-of-the-art facilities in Rochester offer unparalleled resources for translational research across oncology, cardiology, and neurology.
We provide comprehensive training in GCP/ICH guidelines, REDCap systems, and FDA compliance. With competitive benefits including tuition reimbursement and flexible scheduling, this role offers exceptional career growth in one of America's top healthcare systems.
Responsibilities
- Manage complex clinical trial protocols from initiation to closeout, ensuring FDA and ICH compliance
- Recruit, screen, and enroll participants while maintaining rigorous ethical standards
- Coordinate multidisciplinary teams including physicians, nurses, and biostatisticians
- Maintain accurate electronic data capture in REDCap and clinical trial management systems
- Prepare regulatory submissions and monitor adverse events per SOPs
- Train staff on study protocols and conduct source document verification
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- Certified Clinical Research Coordinator (CCRC) or equivalent certification
- Minimum 3 years clinical trial coordination experience in therapeutic areas
- Proficiency in EDC systems (e.g., Medidata Rave, Oracle Inform)
- Demonstrated knowledge of GCP, FDA 21 CFR Part 812, and ICH guidelines
- Exceptional organizational skills with attention to regulatory detail
- Strong communication abilities for stakeholder management and patient education