Job Description
Join Mayo Clinic's elite Clinical Research Division as a Senior Clinical Research Coordinator. Lead groundbreaking studies in oncology, cardiology, or neurology while ensuring protocol compliance and regulatory excellence. Collaborate with world-class physicians and contribute to life-changing medical innovations.
We offer competitive compensation, comprehensive benefits, and opportunities for professional development in one of America's top healthcare institutions.
Responsibilities
- Design and manage complex clinical trial protocols from initiation to closure
- Oversee site compliance with FDA regulations and GCP standards
- Coordinate multi-disciplinary research teams including physicians, nurses, and data analysts
- Monitor patient safety data and adverse event reporting
- Develop and maintain IRB submissions and regulatory documentation
- Analyze trial data and prepare comprehensive study reports
- Mentor junior research coordinators
Qualifications
- Master's degree in Life Sciences, Nursing, or related field
- 5+ years clinical research coordination experience
- Certified Clinical Research Professional (CCRP) or equivalent
- Expertise in oncology or cardiology research protocols
- Proficiency with electronic data capture systems (e.g., Medidata Rave)
- Demonstrated leadership in multi-center trials
- Strong knowledge of 21 CFR Part 11 and ICH-GCP guidelines
- Excellent written and verbal communication skills