Rachael Sarpong

Clinical Trial Coordinator at UCL
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Contact Information
us****@****om
(386) 825-5501
Location
UK

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Experience

    • United Kingdom
    • Research Services
    • 700 & Above Employee
    • Clinical Trial Coordinator
      • Sep 2016 - Present

    • United Kingdom
    • Higher Education
    • 700 & Above Employee
    • Study Coordinator
      • Apr 2015 - Aug 2016

      -Responsible for the day-to-day coordination of a non-CTIMP Breast Cancer study. -Remote monitoring -Data cleaning -Writing Standard Operating Procedures, Guidelines and Work Instructions. -Co-ordination of PPI group -Co-ordinating the re-collection of pathology samples -Responsible for the day-to-day coordination of a non-CTIMP Breast Cancer study. -Remote monitoring -Data cleaning -Writing Standard Operating Procedures, Guidelines and Work Instructions. -Co-ordination of PPI group -Co-ordinating the re-collection of pathology samples

    • United States
    • 1 - 100 Employee
    • Late Phase Research Assistant
      • Jan 2015 - Apr 2015

      -Maintaining study documents and CTMS database -Disseminating project materials to sites and contractors -Coordinating projected related communications with UK & international project team -Maintaining study documents and CTMS database -Disseminating project materials to sites and contractors -Coordinating projected related communications with UK & international project team

    • United Kingdom
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Trials Assistant
      • Jun 2013 - Jan 2015

      -Assisting with study management for Phase II & III commercial multi-centre studies -Data entry and resolution of data queries onto study specific databases -Day-to-day liaison with nursing team, PIs, internal and external support services -Handling, processing and dispatch of clinical samples -Maintaining and updating study documents -Preparation of assigned study kits -Assisting with study management for Phase II & III commercial multi-centre studies -Data entry and resolution of data queries onto study specific databases -Day-to-day liaison with nursing team, PIs, internal and external support services -Handling, processing and dispatch of clinical samples -Maintaining and updating study documents -Preparation of assigned study kits

    • United Kingdom
    • Hospitals and Health Care
    • 700 & Above Employee
    • CSP Administrator
      • Aug 2012 - Jun 2013

    • United Kingdom
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Trials Administrator
      • Mar 2012 - Aug 2012

Education

  • Kingston University
    Medicinal Chemistry, Chemistry
    2003 - 2006

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