Job Description
Join Mayo Clinic's world-renowned oncology research team as a Clinical Research Coordinator. You'll be pivotal in advancing cancer treatments through meticulous trial coordination, ensuring compliance with FDA regulations, and collaborating with multidisciplinary specialists. This role offers unparalleled growth in a supportive environment at a top-ranked medical institution.
Responsibilities
- Design and implement oncology clinical trial protocols in compliance with FDA and ICH-GCP standards
- Recruit, screen, and enroll eligible patients while maintaining ethical research practices
- Manage complex data collection, including adverse event reporting and lab result tracking
- Coordinate cross-functional teams including oncologists, biostatisticians, and regulatory affairs
- Prepare regulatory submissions and maintain audit-ready documentation systems
- Train staff on SOPs and ensure ongoing protocol adherence
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in oncology
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in electronic data capture systems (e.g., REDCap, Medidata Rave)
- Deep understanding of oncology clinical trial methodologies and endpoints
- Exceptional organizational skills with attention to regulatory compliance
- Strong communication abilities for patient education and stakeholder collaboration