Department OverviewThis position will support the quality assurance system (QMS) at the Casey Reading Center (CRC) related to their ongoing clinical research studies. Responsibilities will involve document management according to the QMS and ensuring regulatory compliance. In addition, understanding the applications to ensure validation is performed successfully, assist with clinical study questions to ensure quality systems are followed, oversee policies and procedure documents, and establish additional checkpoints to ensure data integrity. Ensure performed comply with International Conference on Harmonization, Good Clinical Practices, FDA 21 CFR Part 11, and The EU General Data Protection Regulation (GDPR). This position is authorized to work remotely to fulfill t