Georgiana Browne

Experience

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  Royal Air Force Volunteer Reserve (Training)

  Jan 2009 - Jan 2011

  Officer Cadet
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  The Disabilities Trust

  Aug 2012 - Apr 2013

  Psychology Assistant
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  University of Exeter Medical School

  Apr 2013 - Sept 2013

  Honorary Research Assistant
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  NHS Trust

  Nov 2014 - Oct 2019

  Band 6 research practitioner -Set up and lead multiple mental health clinical trials (Dementia, Psychosis, Autism, carer well being and older people), adhering to the conduct set out in ICH-GCP. Conduct thorough feasibility investigations, advanced screening procedures and utilising Patient and Public Involvement and Engagement (PPIE) to ensure studies recruit to time and target.Provide cognitive rating for commercial trials for sponsors.Principal Investigator for a randomised controlled trial with ultimate responsibility for the conduct of the study.Line manage a team of junior staff, providing them with training and support enabling them to provide invaluable assistance to the recruitment and follow up of Devon Partnership NHS Trust's (DPT) trial portfolio.The Equality, Diversity and Inclusion (EDI) lead for Research and Development (R&D). I contribute to producing EDI policies for DPT, attend quarterly EDI update meetings and disseminate information about current legislation, policies and EDI events amongst R&D. Show less Coordinated two global commercial phase 3 clinical trials which recruited to time and target. Carried out follow up assessments and coordinated the local medical teams, cognitive raters and vendors associated with the respective studies. Maintained and carried out extensive site file review and source document checks to ensure that the quality of our records and data were in accordance to ICH-GCP and study protocol. Conducted source data verification such as frequent cross referencing of source documents with data on electronic data capture systems.Completed source data review, implementing processes to ensure the quality of our site's source data. This included designing local Standard Operating Procedures (SOPs) for data collection and protocol specific worksheets based on the eCRF.Facilitated site monitoring, ensuring that all study documentation including the site file and source documents are complete and available. Assisted study CRAs’ by providing site protocol and cognitive rating training for staff employed after the study Site Initiation Visits. Show less

  • Senior Research Practitioner

    Dec 2017 - Oct 2019

  • Research Practitioner

    Aug 2016 - Dec 2017

  • Clinical Trial Administrator

    Oct 2014 - Jul 2016

  • Research Assistant Practitioner

    Nov 2014 - Mar 2016
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  Newcastle University

  Oct 2019 - Apr 2021

  Clinical Trials Manager

  I am a Trial Manager within the Newcastle Clinical Trials Unit (NCTU). I currently work on a number CTIMP trials. As a Trial Manager I support investigators and sites with the development, set-up, monitoring and close-down of clinical trials.

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  IQVIA

  Apr 2021 - now

  • Senior Global Trial Manager/ Strategy and Operations Manager (Novartis FSP)

    Apr 2023 - now

  • Global Trial Manager (Novartis FSP)

    Apr 2021 - Apr 2023
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  STEM Ambassadors

  Jan 2023 - now

  STEM Ambassador