Olayinka Sholaja

Project Coordinator at IMAGE ANALYSIS GROUP (IAG)
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Contact Information
us****@****om
(386) 825-5501
Location
London, England, United Kingdom, GB
Languages
  • French -

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Credentials

  • GCP
    -

Experience

    • United Kingdom
    • Venture Capital and Private Equity Principals
    • 1 - 100 Employee
    • Project Coordinator
      • Jul 2019 - Present

    • United Kingdom
    • Education Management
    • 1 - 100 Employee
    • Student Mentor
      • Jan 2017 - Present

      Volunteer Student Mentor Volunteer Student Mentor

    • United Kingdom
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Clinical Research Technician
      • Sep 2016 - Sep 2017

      Therapeutic Area (Respiratory Diseases)- COPD-Asthma Therapeutic Area (Respiratory Diseases)- COPD-Asthma

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Research Assistant
      • Oct 2015 - Sep 2016

      Alert medical staff immediately of any untoward medical occurrence suffered by a study participant Appropriately and within the scope of your training deal with any medical emergency arising in the Unit until a nurse and/or physician arrive at the scene  Assist in the timely review of protocols, ICFs, study procedure manuals, CRFs and other supplements to the protocol in draft and final versions for correctness, clarity and operational feasibility  Assist in the review and comment of Clinbase set up and perform dummy runs for assigned studies.Prepare all study related documentation, including generating any study specific forms and worksheets  Organise ward set-up to ensure appropriate preparation for study admission e.g. sufficient number of working Clinbase stations, ECG leads, BP cuffs, blood sampling tubes, urine containers and other required materials  Admit and orientate study participants within the Unit and deliver study specific presentation  Perform acquisition of ECG and blood pressure measurements Perform venepuncture and cannulation for blood sampling  Prepare required devices and study participants for Holter/Telemetry monitoring as per protocol requirements  Obtain urine and faecal collections as per protocol requirements Assist in compiling appropriate responses to internal and sponsor data queries and audit observations in a timely manner  Participation in internal and external meetings as required  Undertake any tasks that your line manager/Department Head may require from you within your scope of work  Maintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner  Participate in formal staff review processes e.g. performance and salary reviews to corporate standards and timescales Skills

Education

  • Queen Mary University of London
    Master of Science (MSc), Clinical Drug Development
    2016 - 2017
  • Royal Holloway, University of London
    Bachelor’s Degree, Biomedical Sciences
    2011 - 2015
  • DCA Home Learning
    Diploma (Level 3), Pharmacy Technician/Assistant
    2013 - 2013
  • Sacred Heart School, Republic of Ireland
    Irish Leaving Certificate
    2007 - 2011

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