Position Summary
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.
Required Experience
1 year
Work Schedule
TBD by Supervisor
Required Experience:
IC