Job Description
Join Mayo Clinic's prestigious clinical research division as a Senior Clinical Research Coordinator. Lead groundbreaking studies in oncology while ensuring regulatory compliance and patient safety. Our state-of-the-art facilities in Rochester offer unparalleled resources for innovative medical research.
Responsibilities
- Oversee complex clinical trial protocols and ensure FDA/ICH-GCP compliance
- Manage study budgets, timelines, and vendor relationships
- Train and mentor junior research coordinators
- Develop and maintain regulatory documentation (IRB submissions, informed consent forms)
- Collaborate with multidisciplinary teams including physicians, biostatisticians, and data managers
- Analyze and interpret clinical trial data for study reports
- Implement risk-based monitoring strategies for site quality assurance
Qualifications
- Master's degree in life sciences, nursing, or related field
- 5+ years of clinical research coordination experience
- Certified Clinical Research Professional (CCRP) certification
- Expertise in oncology trial protocols and adverse event management
- Advanced proficiency in electronic data capture systems (e.g., Medidata Rave)
- Strong knowledge of FDA 21 CFR Part 312 regulations
- Demonstrated project management skills with complex multi-center trials
- Excellent written and verbal communication abilities