Seeking a full-time Data Management Specialist to provide data management support for Investigator Initiated Trials, utilizing OnCore for protocol calendar specifications and eCRFs, while collaborating with research staff in a hybrid work environment. Key responsibilities Manage data collection processes throughout the study life cycle in collaboration with various protocol staff Build protocol calendar specifications and develop electronic case report forms (eCRFs) using OnCore Ensure adherence to clinical trials design and data management processes within the oncology therapeutic area Required qualifications Bachelor's degree in a relevant field Three years of related experience in data management or clinical trials Knowledge of electronic data capture (EDC) systems and forms design Understanding of clinical trial processes and oncology No specific licenses or certifications required