• Interpreting clinical data according to medical standards, GCP guidelines, study protocols, charter definitions, and Clario SOPs • Completing source documents accurately and promptly per protocol and SOP requirements • Correcting entries on source documents and Case Report Forms (CRFs) in a timely manner • Participating in protocol‑specific and ongoing training • Performing Photo Image Quality Assessment (Photo IQA) and participating in the medical photography process • Reviewing protocols, charters, and associated clinical and technical documents • Maintaining security and confidentiality of images, data, equipment, study materials, and subject information • Participating in sponsor site visits and audits as needed • Collaborating with management to address and resolve oncology‑related study concerns • Maintaining continuing professional medical education • Conducting quality control to ensure completeness and accuracy of assigned work • Identifying and supporting performance improvement initiatives • Contributing to the development, review, and evaluation of SOPs and study‑specific procedures • Creating oncology‑specific test cases for training • Maintaining a safe work environment and promptly reporting hazards • Participating in the Medical Affairs lecture series • Performing other duties as assigned by Medical Affairs leadership