The Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinical trials and works in conjunction with a Clinical Research Nurse/Coordinator (CRN/CRC) to ensure accurate and timely delivery of data compilation and submission. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families, in a manner that supports the conduct of clinical trials.
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Job Type
Full-time
Career Level
Mid Level