About this role
SPVR NON THERAPEUTIC RESEARCH OPS at Moffitt. Location: Tampa, Florida, United States. Role: supervising staff, overseeing operations, managing studies Requirements: Bachelor's in science/health required (Master's preferred), 3+ years clinical/observational research experience, supervisory experience preferred, knowledge of clinical trial coordination, regulatory compliance and GCP; preferred research certifications CCRP/CCRC/ACRP. Category: Research and Development (R&D) Seniority: Mid Level Certifications: ccrp, ccrc, acrp Commitment: Full Time Workplace: Onsite Languages: English