About this role
Clinical - Clinical Research Coordinator at Tog. Location: Greenville, South Carolina, United States. Role: conducting trials, obtaining consent, managing documentation Requirements: Conduct phase II-IV clinical trials, obtain informed consent, perform medical record review, protocol compliance, blood draws and investigational product administration; CMA certification or willingness to complete; strong medical terminology and data management skills. Category: Healthcare Services - Allied Health Seniority: Entry Level Certifications: cma Commitment: Full Time Workplace: Onsite Languages: English