Job Description
Join Mayo Clinic's prestigious Clinical Research Division as a Senior Clinical Research Coordinator. You'll lead complex multi-center trials in oncology, ensuring protocol compliance, data integrity, and regulatory adherence. Collaborate with world-class physicians, biostatisticians, and pharmaceutical partners to advance groundbreaking treatments.
We offer competitive compensation, comprehensive benefits, and unparalleled professional development opportunities in a globally recognized medical environment.
Responsibilities
- Oversee end-to-end execution of Phase II-III oncology clinical trials across 3+ sites
- Ensure GCP/ICH compliance and maintain FDA/IRB documentation
- Train and mentor junior CRCs and research staff on protocol procedures
- Analyze and report adverse events per FDA guidelines
- Collaborate with biostatisticians on data quality and endpoint validation
- Manage investigator meetings and cross-functional trial communications
Qualifications
- Bachelor's in Nursing or Life Sciences (Master's preferred)
- 5+ years clinical research coordination in oncology/hematology
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Expertise in Oracle RDC and Medidata Rave systems
- Proven track record in multi-center trial management
- Strong knowledge of FDA 21 CFR Part 312 regulations
- Exceptional written and verbal communication skills