Job Description
Join Mayo Clinic's prestigious research division as a Senior Clinical Research Coordinator. Lead groundbreaking studies in oncology while working with world-class physicians and cutting-edge technology. Enjoy comprehensive benefits including flexible scheduling, tuition reimbursement, and wellness programs. This hybrid role offers 3 remote days/week with on-site collaboration at our state-of-the-art Rochester campus.
Responsibilities
- Oversee complex multi-center oncology clinical trials from protocol to closeout
- Manage regulatory documentation (FDA submissions, IRB approvals)
- Train and mentor junior research staff on GCP compliance
- Coordinate investigator meetings and stakeholder communications
- Analyze trial data and prepare regulatory submissions
- Implement electronic data capture systems (EDC) optimization
- Ensure protocol adherence through source document verification
Qualifications
- Master's degree in clinical research or related field
- 5+ years of oncology clinical trial coordination experience
- Certified Clinical Research Professional (CCRP) credential
- Expertise in FDA 21 CFR Part 312 regulations
- Advanced proficiency in Medidata Rave or equivalent EDC systems
- Proven budget management for multi-million dollar trials
- Strong leadership experience with cross-functional teams
- Experience with biostatistical analysis software (SAS, R)