Patrice Deroy

Experience

• 

  Centre Hospitalier Universitaire de Montreal

  Aug 2005 - Dec 2006

  Research Coordinator

  Coordinated intensive care research and development activities Prepared ethics submissionsPlanned and supervised events for the protocol underway with team members, the subject and the related familiesServed as the key figure for the subjects, the families and the various interdisciplinary team membersActed as the key person for private partnersRequested consent from the families and the subjectsPlanned and provided clinical follow-ups, educated and supported the subjects and their familiesEnsured the subject’s needs and expectations are met Warranted to follow Guide to Good Clinical Practices and the schedule for each protocols Recorded observations and interventions in the subject fileConducted open ended interviews with study participantsManaged research budgetsProvided team with necessary trainings for the various protocolsEvaluated the effectiveness and application of the protocols and carried out any required correctionsLiaised between the intensivists and the other clinical partnersManaged the drugs under study in collaboration with the research pharmacistsMet with the CRA during external or internal auditsMaintained and archived documents of the completed projects Developed system tools to collect statistical data for the academic protocolsCollected data and database entries for various research projectsContributed to the developments and revision of specific proceduresPiloted specific projects in collaboration with other clinical partners Show less

• 

  Sacré-Coeur Hospital, Montreal

  Aug 2009 - Apr 2011

  Research Coordinator

  Coordinated intensive care research and development activities Prepared ethics submissionsPlanned and supervised events for the protocol underway with team members, the subject and the related familiesServed as the key figure for the subjects, the families and the various interdisciplinary team membersActed as the key person for private partnersRequested consent from the families and the subjectsPlanned and provided clinical follow-ups, educated and supported the subjects and their familiesEnsured the subject’s needs and expectations are met Warranted to follow Guide to Good Clinical Practices and the schedule for each protocols Recorded observations and interventions in the subject fileConducted open ended interviews with study participantsManaged research budgetsProvided team with necessary trainings for the various protocolsEvaluated the effectiveness and application of the protocols and carried out any required correctionsLiaised between the intensivists and the other clinical partnersManaged the drugs under study in collaboration with the research pharmacistsMet with the CRA during external or internal auditsMaintained and archived documents of the completed projects Developed system tools to collect statistical data for the academic protocolsCollected data and database entries for various research projectsContributed to the developments and revision of specific proceduresPiloted specific projects in collaboration with other clinical partners Show less

• 

  McKesson Canada

  Aug 2011 - Apr 2015

  Bilingual Clinical Research Associate
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  AstraZeneca

  Apr 2015 - now

  • Local Study Associate Director

    Jun 2023 - now

  • Moniteur

    Apr 2015 - Jun 2023