Deputy EU QPPV and EU QPPV

Use your strong Pharmacovigilance background to join our multi-national client CRO's

Rate Full company benefits Industry Life Sciences Location France - Paris Type Permanent Ref JO-1612-899316 Posted 62 days ago

Job Description

The Hydrogen Group is looking for an exceptional candidate to join their international client as an EU QPPV. This multi-national client is looking for someone with a strong Pharmacovigilance background to join their CRO. 

EU QPPV 
THE ROLE:

 

  • Qualified to act as local Qualified Person for Pharmacovigilance (QPPV) in France
  • Project management on drug safety/pharmacovigilance projects
  • Operational management of internal project team and of communications with Clients
  • Implementation/design of appropriate drug safety/pharmacovigilance systems for Clients
  • Involvement in coordination/preparation/review of Safety Management Plans
  • Coordination of EudraVigilance registration of Sponsors/MAHs in Europe
  • Participation in collection and management of SAEs and/or Spontaneous Reports process
  • Involvement in quality control activities
  • Preparation/review/coordination of submission of DSURs/PSURs or other periodic reports
  • Experienced in Maintaining PSMF

EDUCATION REQUIREMENTS AND QUALIFICATIONS:
  • Life science/Medical degree
  • Substantial experience in the pharmaceutical industry 
  • Experience operating within the FR & EU 
  • 5+ years PV experience 
  • Several years of line management experience 
  • Excellent communication skills 
  • Experience operating safety databases and E2B reporting
  • Excellent English and French language skills (additional languages are beneficial) 

Feel free to apply to this position should this role be suited to your skills and experiences. Alternatively you can organise a discussion with a consultant at the Hydrogen Group via telephone.

  #LI-DC2 #LI-15

David Chen Consultant

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+44 (0)20 7002 0000 Get in touch

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