Clinical Therapies Specialist

2 semanas atrás


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Clinical Research Associate Perform site selection, initiation, monitoring and close-out visits of investigational sites for the portfolio of clinical trials. Manage the progress of assigned sites by tracking patient recruitment and enrollment, CRF completion and submission, source data verification, data collection and data query generation and resolution. The Role The Clinical Research Associate will be responsible for overall site conduct. They must have a proficient knowledge of ICH Good Clinical Practice (ICH GCP) regulations and Nexcella SOPs. ,


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