Job Description
Join Mayo Clinic's prestigious Oncology Research Department as a Clinical Research Coordinator. You'll be pivotal in advancing cancer treatment protocols through meticulous trial management, regulatory compliance, and patient advocacy. This role offers unparalleled exposure to cutting-edge oncology research while supporting multidisciplinary teams in a world-class medical environment.
Responsibilities
- Coordinate multi-phase oncology clinical trials including protocol development, patient recruitment, and data collection
- Ensure compliance with FDA regulations, GCP standards, and institutional IRB protocols
- Manage electronic data capture systems and maintain accurate trial documentation
- Serve as primary liaison between investigators, sponsors, and research participants
- Monitor adverse events and implement corrective action plans per SOPs
- Conduct investigator site visits and prepare regulatory submissions
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Minimum 3 years oncology clinical trial coordination experience
- Proficiency in electronic data capture systems (e.g., Medidata Rave)
- Demonstrated knowledge of ICH-GCP and FDA 21 CFR Part 812
- Strong ethical decision-making and crisis management abilities