Travel CRC for Multi-Site Clinical Trials
Alcanza Clinical Research
Alcanza Clinical Research is seeking a Clinical Research Coordinator to support multi-site, multi-phase trials in the United States. You will ensure compliant execution with FDA, GCP, HIPAA, and ICH guidelines under the Site Manager/Director and Principal Investigators. Responsibilities include patient screening, consents, visits, data entry, vital signs, ECGs, AE reporting, and coordination with sponsors; travel may be required. #J-18808-Ljbffr Alcanza Clinical Research
Vacancy posted 1 day ago
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