The Senior Medical Informatics Specialist will lead the delivery of medical consults in the oncology space and work with stakeholders to build real-world evidence to support decisions. The position requires experience in oncology clinical workflows and using longitudinal health records to advance care. This role serves as a human-technology interface and is a full-time remote position.

Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Coordinate all necessary activities required to set up and monitor a study. Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope.

As a CRA II, you will monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas. The CRA is the main sponsor representative, providing key project updates, collaborating with the team, and developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. You will review source to CRF/eCRF, ensuring patient safety and data integrity. You will also oversee the sites' adherence to GCP/ICH practices.