Tamara Kokaz

Medical Affairs Director at Pleco Therapeutics BV
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Contact Information
us****@****om
(386) 825-5501
Location
UK
Languages
  • English Native or bilingual proficiency
  • Arabic Native or bilingual proficiency
  • Spanish Limited working proficiency
Skills

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Bio

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Credentials

  • First Line Managers
    ILM
    Jun, 2022
    - Sep, 2024
  • Mental Health First Aider
    Mental Health First Aid (MHFA) England
    Oct, 2021
    - Sep, 2024
  • Advanced medical information skills
    PIPA - Pharmaceutical Information and Pharmacovigilance Association
    Jul, 2021
    - Sep, 2024
  • Orphan Drugs Clinical Trials
    Symmetric Training

Experience

  • Pleco Therapeutics BV
    • Netherlands
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Medical Affairs Director
      • Jan 2023 - Present
  • Consilient Health
    • Ireland
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Head of Pharmacovigilance & Medical Information
      • May 2021 - Dec 2022
  • Roche
    • Switzerland
    • Biotechnology Research
    • 700 & Above Employee
    • Pharmacovigilance Partnering Specialist
      • Aug 2020 - May 2021
  • Norgine
    • Netherlands
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Pharmacovigilance Audit Manager
      • Mar 2020 - Aug 2020
  • Clinigen Group
    • United Kingdom
    • Chemical Manufacturing
    • 1 - 100 Employee
    • Pharmacovigilance Manager
      • Jul 2016 - Mar 2020

    • Drug Safety Specialist
      • May 2016 - Jul 2016

    • Drug safety and Medical affairs officer
      • Apr 2015 - May 2016

  • Johnson & Johnson
    • Law Practice
    • 1 - 100 Employee
    • Drug Safety Associate, Case Processing, Global Case Management
      • 2014 - 2015
  • Medicines and Healthcare Products Regulatory Agency (MHRA)
    • Pharmacovigilance Service Team Officer
      • May 2013 - May 2014
  • PharSafer
    • United Kingdom
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Pharmacovigilance Officer
      • May 2011 - Dec 2011

      • Data entry onto company validation database • Review of safety information from clinical trials and post marketed products • Paper reporting of ADRs to regulatory agencies • Compliance matrices for clients and company review • Literature searching for ADRs, writing section of periodic safety report (narratives) • Producing summary safety tables for client review • Follow up safety cases to closure, adverse event case file productions and archiving • Understanding and helping with determining ADR reparability • Attendance at business development meeting concerning possible clients • Filing of cases and source documents • Reporting cases according to reporting plan to countries around the world

Education

  • Queen Mary University of London
    Master of Science (MS) Clinical Drug Development, Clinical and Industrial Drug Development
  • Kingston University
    Bachelor of Science (BSc), Pharmacology
  • Kingston College
    Higher National Diploma in Biomedical Sciences, Chemistry, physics, biology
    2006 - 2008

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