Job Description
Join Mayo Clinic's prestigious Clinical Research Department as a Senior Clinical Research Coordinator. Lead groundbreaking studies in oncology while ensuring regulatory compliance and data integrity. We offer competitive compensation, comprehensive benefits, and opportunities for professional growth in a world-class medical environment.
Responsibilities
- Design and implement clinical trial protocols in compliance with FDA/ICH guidelines
- Recruit, screen, and enroll study participants with precision and empathy
- Manage complex data collection systems ensuring 99% accuracy
- Serve as primary liaison between investigators, sponsors, and regulatory bodies
- Mentor junior staff and optimize research workflows
- Prepare comprehensive regulatory submissions and audit documentation
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 3+ years of oncology clinical trial coordination experience
- Certified Clinical Research Professional (CCRP) or equivalent
- Expertise in REDCap, Oracle Clinical, or similar EDC systems
- Proven track record in FDA audit preparation
- Exceptional communication and stakeholder management skills
- Knowledge of 21 CFR Part 11 and GCP standards