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Oncology Research Coord Ii
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- Realigning our MD Anderson Research Department at Cooper University Health Care with the MD Anderson Cancer Center at Houston's recommendation, allows research growth in both the structure and the types of studies we are able to offer our clients to advance care.
- The role of the Oncology Research Coordinator II provides the oversite of clinical studies in the oncology setting managing treatment trials including Phase 1-1V- multi drug regimens, high toxicity potential immunotherapies, cell therapies.
- Completes and maintains the relevant research training to function in the role- including EPIC training, EPIC billing, CITI, GCP, and Specimen Handling.
- Completes and maintains the oncology study specific training required to work on assigned trials- not limited to electronic data bases, scan portals, lab portals, protocol training and amendment training.
- Organize and maintain all documentation required by the sponsor or CRO per GCP - includes source documentation (including the electronic medical record system, EPIC), case report forms, and research charts.
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