Pharmacovigilance expert (post authorisation) to help with documentation for registration dossier

  • Belgium
  • from 61 /hour
  • 0 %
  • Expired
  • 704 days ago
  • 60

Domains of expertise

  • Medical Affairs and Pharmacovigilance
    • Drug Safety Officer/Associate
    • Drug Safety Physician
    • Medical Advisor
    • Medical Writer
    • Pharmacovigilance and drug database administrator
    • Other Expert
  • Pharmacy
    • Pharmacist

Description

the mission is to support with writing a pharmacovigilance document for a generic combination product.

Skills required

medical writing, more specifically for Drug registration and pharmacovigilance purposes (PSUR and RMP...), experience required. Knowledge of current EU guidance/GVP etc is a must. 

  • Company Type

    Pharmaceutical

  • Mission location(s)

    • Europe
      • Belgium
        • Brussels
        • Flanders region
          • Antwerp
          • East Flanders
          • Flemish Brabant
          • Limburg
          • West Flanders
        • Walloon region
          • Hainaut
          • Liège
          • Luxembourg
          • Namur
          • Walloon Brabant
    The Freelancer is free to reside in any location for this mission
  • Mission start date

    10/01/2018

  • Education degree

    Life sciences Master degree, such as pharmacist, medical doctor, biomedical sciences

  • Experience level

    4 - 10 Years experience in this/these domain(s)

  • Fee proposed

    from 61 /hour (Euro)

  • Reference number

    171210-12001-CORTEX-53115
  • Contract duration

    3 day(s)

  • Contract renewal?

    can be renewed