Laboratory Technician And Clinical Trial Assistant | Service Provider
Current- Complies with the applicable legal, ethical and regulatory requirements, applicable Standard Operating Procedures (SOPs) and business ethics.- Completes the project-specific Case Report Form (CRF) on a timely manner and in compliance with the ICH-GCP ALCOA++ principles- Performs the quality control (QC) of the completed project-specific source documents- Performs all the corrections required to the completed project-specific source documents on a timely manner- Fully adheres to the Clinical Trial Coordinator instructions and maintains the Phase I study participants’ database updated and organized- Processes and storages biological samples according to the appropriate methodology- Performs safety laboratory urine dipstick tests and produces the corresponding laboratory report- Processes safety laboratory samples and delivers them to the laboratory of Hospital da Prelada.
