Job Description
Join Mayo Clinic's prestigious research division as a Clinical Research Coordinator and shape the future of medicine. In this pivotal role, you'll manage complex clinical trials from protocol development to FDA submission, ensuring regulatory compliance and data integrity. Collaborate with world-class physicians, scientists, and pharmaceutical partners to advance breakthrough treatments in oncology and cardiology. Mayo offers unparalleled professional development, cutting-edge resources, and a culture centered on patient care and innovation.
Responsibilities
- Design, implement, and oversee clinical trial protocols in compliance with FDA and ICH-GCP standards
- Recruit, screen, and enroll participants while maintaining ethical research practices
- Manage electronic data capture systems and ensure accurate data collection/analysis
- Coordinate multidisciplinary research teams and maintain investigator relationships
- Prepare regulatory submissions and maintain comprehensive trial documentation
- Monitor adverse events and ensure patient safety protocols are followed
- Present findings at scientific conferences and contribute to peer-reviewed publications
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience in oncology/cardiology
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Expertise in electronic data capture systems (e.g., Medidata Rave, Oracle Inform)
- Deep understanding of FDA 21 CFR Part 11 and ICH-GCP guidelines
- Exceptional organizational skills with attention to regulatory detail
- Strong written communication for protocol development and reporting
- Experience managing investigator-initiated trials and IND applications