Job Description
Join Mayo Clinic's prestigious Clinical Research team as a Senior Clinical Research Coordinator. Lead groundbreaking studies in oncology, cardiovascular research, or neurology at one of America's top-ranked medical institutions. Enjoy competitive benefits, cutting-edge facilities, and collaborative partnerships with world-renowned physicians. Your expertise will directly impact patient care advancement through meticulously managed clinical trials.
Responsibilities
- Design, implement, and oversee complex multi-site clinical trials from protocol development to final reporting
- Recruit, screen, and maintain subject cohorts ensuring strict adherence to GCP and FDA regulations
- Manage comprehensive trial documentation including CRFs, adverse event reporting, and regulatory submissions
- Coordinate cross-functional teams including biostatisticians, data managers, and principal investigators
- Analyze and interpret clinical data to generate actionable insights for protocol modifications
- Mentor junior CRCs and conduct staff training on SOPs and regulatory compliance
Qualifications
- Master's degree in Clinical Research, Nursing, Life Sciences, or related field
- Certified Clinical Research Professional (CCRP) or ACRP-CP certification required
- Minimum 5 years of clinical trial coordination experience in therapeutic areas
- Proven expertise in EDC systems (e.g., Medidata Rave, Veeva Vault)
- Demonstrated success in managing Phase II-III oncology or cardiovascular trials
- Strong knowledge of ICH-GCP, FDA 21 CFR Part 812, and HIPAA compliance
- Exceptional project management skills with ability to meet aggressive deadlines