Job Description
Join Mayo Clinic's world-class oncology research team as a Clinical Research Coordinator. You'll play a pivotal role in advancing cancer treatments while ensuring regulatory compliance and patient safety. This position offers unparalleled opportunities to work with cutting-edge therapies and multidisciplinary experts in a globally recognized medical institution.
Responsibilities
- Oversee clinical trial protocols including IRB submissions, informed consent processes, and regulatory documentation
- Coordinate patient recruitment, screening, and enrollment for oncology clinical trials
- Manage trial data collection, quality control, and reporting to sponsors and regulatory bodies
- Serve as primary liaison between research teams, sponsors, and regulatory authorities
- Monitor adverse events and ensure compliance with GCP and FDA regulations
- Train and mentor junior research staff on protocol procedures and regulatory requirements
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- Certified Clinical Research Coordinator (CCRC) or equivalent certification
- Minimum 3 years of clinical research experience in oncology or oncology trials
- Proficiency with electronic data capture systems (e.g., Medidata Rave) and EHRs
- Deep knowledge of FDA regulations, ICH-GCP, and 21 CFR Part 11
- Exceptional organizational skills and attention to detail in complex trial management
- Strong interpersonal skills for patient interaction and team collaboration