Pharmacovigilance Drug Safety
Atria Biosciences
5d ago

Role :

  • Processing of adverse events reports originating different region and source.
  • Project Monitor and manage the client relation for PVG .
  • Additional responsibility to be a contact to the client in absence of Team lead .
  • Make sure all the process are as per SOP and timelines.
  • Case processing, triage and narration writing skills
  • Involve in preparation for audits / inspections.
  • Should have strong knowledge of EU vigilance systems.
  • Should have a valid passport to travel Europe
  • Eligibility criteria :

  • Bachelors / Master Degree in Pharmacy
  • Excellent English communication skills both written and verbal.
  • Fully aware of current Pharmacovigilance regulations and legislation.
  • Project Management skills; good organisational, planning, co-ordination, follow up skills.
  • Strong software learning skills, and willing to update skillset.
  • Apply
    Add to favorites
    Remove from favorites
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form