Hasan Mert Bozkuş

Experience

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  ATLASCRO

  May 2016 - Nov 2017

  Clinical Research Site Coordinator

  - Support investigators in the protocol complience- Support investigators in the informed consent process- Support investigators actively in subject recruitment .(source data recording)- Support investigators actively in the safety evaluation process- Record subject data on CRFs if delegated by investigator- Organise subject visit schedules according to the study protocol- Filing all correspondences received from the sponsor and the ethics committee to the principal investigator's file- Within the authorization of the coordinator physician, to help entering data obtained from volunteers completely and truly to printed or electronic case report forms (e-CRF) volunteer file and screening cards- Sending blood samples drawn from volunteers to central or local laboratory as per the trial protocol, organization, tracking of courier procedures , monitoring laboratory reports, making the investigator or physician or dentist examine reports, filing reports informing those concerned for taking immediate measure if there is a remarkable or labeled abnormal finding in the report.- Taking necessary measures in order to ensure adequate amount of study materials,patient diaries , laboratory kits, patient identification cards and is available throughout the study.- Relevant form for safety notifications which fulfill definition of serious adverse event reported by the volunteers is filled in by the investigator who is principal investigator or physician or dentist and it is immediately notified to the sponsor and monitoring such events. Show less

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  MediSMART Contract Research Organization

  Nov 2017 - Aug 2018

  Clinical Research Coordinator
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  MyCRO

  Aug 2018 - Jan 2019

  Clinical Research Coordinator

  - Support investigators in the protocol complience- Support investigators in the informed consent process- Support investigators actively in subject recruitment .(source data recording)- Support investigators actively in the safety evaluation process- Record subject data on CRFs if delegated by investigator- Organise subject visit schedules according to the study protocol- Filing all correspondences received from the sponsor and the ethics committee to the principal investigator's file- Within the authorization of the coordinator physician, to help entering data obtained from volunteers completely and truly to printed or electronic case report forms (e-CRF) volunteer file and screening cards- Sending blood samples drawn from volunteers to central or local laboratory as per the trial protocol, organization, tracking of courier procedures , monitoring laboratory reports, making the investigator or physician or dentist examine reports, filing reports informing those concerned for taking immediate measure if there is a remarkable or labeled abnormal finding in the report.- Taking necessary measures in order to ensure adequate amount of study materials,patient diaries , laboratory kits, patient identification cards and is available throughout the study.- Relevant form for safety notifications which fulfill definition of serious adverse event reported by the volunteers is filled in by the investigator who is principal investigator or physician or dentist and it is immediately notified to the sponsor and monitoring such events. Show less

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  IQVIA

  Jan 2019 - Apr 2020

  • Clinical Research Associate II at Roche through IQVIA cFSP Model

    Feb 2020 - Apr 2020

  • Clinical Research Associate I at Roche through IQVIA FSP Model

    Jan 2019 - Feb 2020
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  Novo Nordisk

  May 2020 - Feb 2022

  Clinical Research Associate
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  Syneos Health

  Feb 2022 - Aug 2022

  Senior Clinical Research Associate
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  ICON plc

  Aug 2022 - now

  • Local Study Manager (Turkiye & Middle East)

    Oct 2023 - now

  • Clinical Quality Lead & Country Safety Lead

    Aug 2022 - Oct 2023