StudyConduct:ClinicalResearchCoordinatorPersonnelModificationStudyTransferChecklistClinicalNoteGuidelineInternalWorkingFolderStudy FileManagementQRGPrincipalInvestigatorInstitutionalReviewBoardOffice ofResearchRegulatorySupport48hoursStudy Conduct-Oversight,Maintenance,and Reporting:Clinical DataAssociateSupervisorand ClinicalResearchCoordinatorStudyConduct-Patient Care:Clinical DataAssociateSubjectFilesPtraxTestSchedule2weeksStudyConduct-Patient Care:Clinical DataAssociateMonitoringConciergeServicesSourceDocumentsResearchNoteContractResearchOrganizationProtocolDevelopmentUnit (PDU)Start Up:ClinicalDataAssociateFood andDrugAdministration(FDA)FalseAssociateResearchProtocolSpecialistCancer:RDMS Non-Caner:eBinerEpicCareLink, SimpleShare andVestigoElectronicMedicalRecordTransitioningStaff: ClinicalResearchCoordinatorRBITStudyConduct:ClinicalResearchCoordinatorPersonnelModificationStudyTransferChecklistClinicalNoteGuidelineInternalWorkingFolderStudy FileManagementQRGPrincipalInvestigatorInstitutionalReviewBoardOffice ofResearchRegulatorySupport48hoursStudy Conduct-Oversight,Maintenance,and Reporting:Clinical DataAssociateSupervisorand ClinicalResearchCoordinatorStudyConduct-Patient Care:Clinical DataAssociateSubjectFilesPtraxTestSchedule2weeksStudyConduct-Patient Care:Clinical DataAssociateMonitoringConciergeServicesSourceDocumentsResearchNoteContractResearchOrganizationProtocolDevelopmentUnit (PDU)Start Up:ClinicalDataAssociateFood andDrugAdministration(FDA)FalseAssociateResearchProtocolSpecialistCancer:RDMS Non-Caner:eBinerEpicCareLink, SimpleShare andVestigoElectronicMedicalRecordTransitioningStaff: ClinicalResearchCoordinatorRBIT

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