ContractResearchOrganizationResearchNoteRBITStudyTransferChecklistAssociateResearchProtocolSpecialistSupervisorand ClinicalResearchCoordinatorTestScheduleStudyConduct:ClinicalResearchCoordinatorProtocolDevelopmentUnit (PDU)Start Up:ClinicalDataAssociateSourceDocumentsOffice ofResearchRegulatorySupportClinicalNoteGuideline48hoursElectronicMedicalRecordPtraxStudy FileManagementQRGStudyConduct-Patient Care:Clinical DataAssociateInternalWorkingFolderInstitutionalReviewBoardFood andDrugAdministration(FDA)2weeksSubjectFilesMonitoringConciergeServicesTransitioningStaff: ClinicalResearchCoordinatorCancer:RDMS Non-Caner:eBinerFalseStudy Conduct-Oversight,Maintenance,and Reporting:Clinical DataAssociatePersonnelModificationStudyConduct-Patient Care:Clinical DataAssociatePrincipalInvestigatorEpicCareLink, SimpleShare andVestigoContractResearchOrganizationResearchNoteRBITStudyTransferChecklistAssociateResearchProtocolSpecialistSupervisorand ClinicalResearchCoordinatorTestScheduleStudyConduct:ClinicalResearchCoordinatorProtocolDevelopmentUnit (PDU)Start Up:ClinicalDataAssociateSourceDocumentsOffice ofResearchRegulatorySupportClinicalNoteGuideline48hoursElectronicMedicalRecordPtraxStudy FileManagementQRGStudyConduct-Patient Care:Clinical DataAssociateInternalWorkingFolderInstitutionalReviewBoardFood andDrugAdministration(FDA)2weeksSubjectFilesMonitoringConciergeServicesTransitioningStaff: ClinicalResearchCoordinatorCancer:RDMS Non-Caner:eBinerFalseStudy Conduct-Oversight,Maintenance,and Reporting:Clinical DataAssociatePersonnelModificationStudyConduct-Patient Care:Clinical DataAssociatePrincipalInvestigatorEpicCareLink, SimpleShare andVestigo

Roles and Responsibilities - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. Contract Research Organization
  2. Research Note
  3. RBIT
  4. Study Transfer Checklist
  5. Associate Research Protocol Specialist
  6. Supervisor and Clinical Research Coordinator
  7. Test Schedule
  8. Study Conduct: Clinical Research Coordinator
  9. Protocol Development Unit (PDU)
  10. Start Up: Clinical Data Associate
  11. Source Documents
  12. Office of Research Regulatory Support
  13. Clinical Note Guideline
  14. 48 hours
  15. Electronic Medical Record
  16. Ptrax
  17. Study File Management QRG
  18. Study Conduct-Patient Care: Clinical Data Associate
  19. Internal Working Folder
  20. Institutional Review Board
  21. Food and Drug Administration (FDA)
  22. 2 weeks
  23. Subject Files
  24. Monitoring Concierge Services
  25. Transitioning Staff: Clinical Research Coordinator
  26. Cancer: RDMS Non-Caner: eBiner
  27. False
  28. Study Conduct-Oversight, Maintenance, and Reporting: Clinical Data Associate
  29. Personnel Modification
  30. Study Conduct-Patient Care: Clinical Data Associate
  31. Principal Investigator
  32. EpicCare Link, Simple Share and Vestigo