Marco Kuik

Experience

• 

  TNO Quality of Life

  May 1998 - Jun 2006

  Resarch analist and Sample coördinator
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  Covance CLS

  Sept 2006 - Nov 2007

  Data coördinator
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  SynCo Bio Partners

  Mar 2008 - Sept 2009

  Sample coördinator
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  Eli Lilly and Company

  Feb 2010 - Nov 2010

  Clinical Trial Assistent

  uitvoeren van administratieve en logistieke taken ter ondersteuining van Clinical trials. Indiening van onderzoeks documenten bij de bevoegde instantie.

• 

  MSD Sharp & Dohme GmbH

  Nov 2010 - Feb 2013

  CTA

  Placed at MSD by ClinTec International Ltd.

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  PRA Health Sciences

  Mar 2013 - Mar 2022

  Currently gaining experience in conducting/monitoring clinical trials for Phase II, III & IV. Ensuring sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH guidelines. Review of patient safety data.Main Responsibilities:Monitoring and management (source data review and verification, patient safety data & informed consent, monitoring reports, filing) of phase II & III NSCLC oncology clinical trial and phase III ADHD & Hepatitis B trial.Initiation, monitoring and management of phase IV brain tumor/epilepsy clinical trial.Monitoring and management of phase II vaccine clinical trial.Training of site staff in the study protocol, eCRF and IxRS system. Show less

  • TitleClinical Research Associate II

    Apr 2020 - Mar 2022

  • Clinical Research Associate ( I )

    Feb 2015 - Apr 2020

  • In-House Clinical Research Associate

    Mar 2013 - Jan 2015
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  UMC Utrecht

  Apr 2022 - now

  Clinical Study Coordinator