Responsible for the collection and review of clinical protocol research data; Interpretation of data (including appropriate source documentation) for entry into computerized databases; Creation of data definitions and case report forms and other information related to data collection for clinical research conducted by Oncology/Hematology investigators. Provide support to the Oncology/Hematology clinical study coordinators through data collection, scheduling, research protocol management, and other administrative duties.
Job Questions? Ask Charlie
