Auditor I, Clinical Quality Assurance

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview Iovance is seeking an Auditor I, Clinical Quality Assurance, who has experience in GCP/GCLP/GVP/GMP compliance in Contract Research Organization (CRO), pharmaceutical and/or biotechnology companies. This individual will be primarily responsible for assisting with GCP investigational site, clinical service provider, trial master file, and GCP internal system