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Job Details
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EU QPPV



Business Type: Pharmaceutical Company, Contract Research Organisation, Pharmaceutical Services
Job Type: Pharmacovigilance
Job Level: Experienced (non manager)
Position: Full Time
Location: Poland
Reference: NS4730
Closing Date: 09/05/19
Job Details:

EU QPPV

Anywhere in Europe- office and homebased

Salary: £Negotiable

INTRO:


A fantastic opportunity has arisen for an experienced EU QPPV to a join a top global CRO. The right candidate will be based within a non-UK EU Member State due to the UK''s future plan to withdraw from the EU.

The suitable candidate will have strong experience in a senior pharmacovigilance role and have strong understanding of EU regulations within PV. This is truly a growing company that offers a chance to work in a variety of clinical trials from Phase I to post-marketing in a variety of therapy areas.

Main responsibilities:

  • Review and oversee the PV system
  • Review of RMPs
  • Acting as single PV contact point for competent authorities in Member States
  • Acting as contact point for PV inspections and supporting these
  • Oversight for conduct of PV and submission of PV related documents

Requirements:

  • Life Science degree
  • Excellent knowledge of ICH, CIOMS and EU guidelines
  • Experience in influencing the PV system
  • Strong previous experience as a QPPV
  • Expert knowledge of PV regulations and GVP guidelines
  • Excellent English communication skills
  • Strong project management skills
  • Experience in PV safety risk management
  • Strong Post-marketing and clinical trial experience

To Apply
If you would like to discuss this vacancy further, please call i-Pharm Recruitment Consultant Niki Sansoy on +44 (0)20 3189 0470 or email nsansoy@i-pharmconsulting.com.

ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.



Posted: 11/04/2019 | NPJ Ref: 233722
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