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Sílvia Martínez Gil

Sílvia Martínez Gil

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location of Sílvia Martínez GilBarcelona, Catalonia, Spain

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  • Timeline

  • About me

    Global Study Manager

  • Education

    • Universidad de Valencia

      2015 - 2017
      Master degree in Pharmaceutical Oncology Medicine

      During the master degree, I acquired and broaden my knowledge about oncology therapy and oncology clinical trials in order to offer high-quality labour conducting clinical trials.

    • Universitat de Barcelona

      2010 - 2014
      Bachelor's degree Biology with a mention in Molecular, Cellular and Systems Biology

      During my bachelor degree, I acquired knowledge about biology but I focused in following areas: Immunology, Neurobiology, Genetic engineering, Metabolism, Cancer biology, Microbiology and Physiology

    • IUSC | International University Study Center

      2014 - 2015
      Master's degree Clinical Trial Monitoring

      During my master's degree, I acquired the necessary knowledge about: Clinical research: drug development, national and international regulatory of clinical trials, initiation and start up in clinical trial, monitoring and close out visit in clinical trial and clinical research in specific areas.

  • Experience

    • ICON plc

      Nov 2014 - Jan 2019

      Identify, select, initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out accordingly to the study protocol and sponsor requirements (Lundbeck, Morphosys, Novartis, Biogen and BMS) and in accordance with SOPs, applicable regulation and the principles of ICH-GCP. - Therapeutic areas: Neurology, Psychiatric (pediatric), oncology (solid tumours, prostate cancer, head and neck cancer,), gastrointestinal system, hematology (lymphoma) Show less

      • CRA II

        Apr 2017 - Jan 2019

      • CRA I

        Mar 2016 - Mar 2017

      • In-house CRA

        Aug 2015 - Mar 2016

      • Clinical Trial Assistant

        Mar 2015 - Aug 2015

      • CRA Trainee

        Nov 2014 - Mar 2015

    • PPD

      Jan 2019 - Oct 2021

      Initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out accordingly to the study protocol and sponsor requirements and in accordance with SOPs, applicable regulation and the principles of ICH-GCP. - Therapeutic areas: hematology (lymphoma, leukemia), neurology Initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out accordingly to the study protocol and sponsor requirements and in accordance with SOPs, applicable regulation and the principles of ICH-GCP. - Therapeutic areas: hematology (lymphoma, leukemia), neurology

      • Senior CRA II

        Apr 2021 - Oct 2021

      • Senior CRA I

        Jan 2019 - Mar 2021

    • Thermo Fisher Scientific

      Oct 2021 - Mar 2024
      Associate Project Manager

      Drive and own a sub-set of project-specific activities as directed by the Project Lead to support overall delivery of the project; compile and present status updates to Leadership; liaise with functional leads to ensure proper financial forecasting and actualization of deliverables, and input for the project Risk Register; assist project teams in the early adoption of new systems or processes; drive team compliance with project-specific requirements; and networks with senior internal and external stakeholders in own area of expertise.On December 8, 2021, Thermo Fisher Scientific completed the acquisition of PPD. Show less

    • AstraZeneca

      Apr 2024 - now
      Global Study Manager

      Responsible for supporting the delivery of clinical studies ensuring quality and compliance.

  • Licenses & Certifications