Jacqueline Perrin

Experience

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  SPECTRUM HEALTH BLODGETT CAMPUS

  Jan 1996 - Jan 1999

  Pharmacy Technician

  Receive and dispense prescriptionsPerform monthly nursing unit inspectionsFacilitated in the implementation of a robot system to dispense medicationsTrained new staff membersPerformed general secretarial duties for the department

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  Spectum Health

  Dec 1996 - Feb 2010

  Clinical Research Coordinator
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  SPECTRUM HEALTH BUTTERWORTH CAMPUS

  Jan 1999 - Jan 2001

  Pharmacy Research Technician

  Prepare and dispense investigational drugs using aseptic techniqueMaintain proper documentation and drug inventory for each research studyMaintain regulatory binders for each research studyCreate instructional pharmacy binders for each study

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  SPECTRUM HEALTH BUTTERWORTH CAMPUS

  Jun 2001 - Mar 2010

  Clinical Research Coordinator

  Work as a member of a clinical research team.Responsible for patient screening, recruitment, consent process, and enrollment for all current IRB approved studiesResponsible for managing patient consent forms, screening documents, source documents, and follow-up visitsMaintain current status of protocolsCollect, record, and submit appropriate data per study guidelinesManage study correspondence with Institutional Review Board

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  METRO HEALTH HOSPITAL

  Mar 2010 - Mar 2012

  Clinical Research Coordinator

  Responsible for patient screening, recruitment, consent process, and enrollment for all current IRB approved studiesResponsible for managing patient consent forms, screening documents, source documents, and follow-up visitsManagement of regulatory documents and drug/device accountabilityCollect, record, and submit appropriate data via electronic case report form (CRF) systems or paper-based CRFs.Manage study correspondence with Institutional Review BoardConduct staff in-services prior to enrolling in new research trials Show less

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  Metro Health

  Mar 2010 - Mar 2012

  Clinical Research Coordinator

  CCRC

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  Michigan State University

  Feb 2012 - now

  HRPP Compliance Analyst/ Human Research Liaison

  Conducts review for Food and Drug Administration (FDA) requirements for investigational new drugs and devices, registration with clinicaltrials.gov, the Health and Insurance Portability and Accountability Act (HIPAA), and other applicable regulations and guidance for all clinical research submitted to the Institutional Review Board (IRB). Provides oversight, administration, implementation, and management of HRL business. Serves as a resource for investigators and study personnel regarding regulatory requirements, policies and procedures for conducting human research. Reviews and monitors human research to assure compliance with approved protocol procedures and all applicable regulations; including conducting site visits to the human research site, followed by submission of written reports to the MSU Human Research Protection Program (HRPP) and the Institutional Review Boards (IRBs), as appropriate. Show less