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Job Details
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Drug Safety Manager

Business Type: Contract Research Organisation
Job Type: Pharmacovigilance
Job Level: Experienced (non manager)
Position: Full Time
Location: Hampshire
Reference: NS42019
Closing Date: 29/04/19
Job Details:

Drug Safety Manager


Location: Farnborough- office based


Salary: Lucrative, plus bonus and benefits

A mid-size growing CRO are looking for an experiences and talented Drug Safety professional to join the close-knit PV team in Farnborough.

The right candidate will assume the responsibility for day-to-day management of PV including line management, project & workflow management and resource prioritisation. Additionally it will be a "hands on position" where there will be involvement in case processing and submissions of ICSRs and SUSARs.

Additional responsibilities include:

  • Line Management of junior Drug Safety Specialists
  • Preparation and submission of PSURs and DSURs
  • Assisting with Signal Detection
  • Benefit Risk Activities
  • Supporting the VP & Director of PV
  • Project Management experience
  • Co-ordinating and assisting with departmental training
  • Assisting in the safety database configuration and management


  • Life Science degree or nursing background
  • Previous experience as a Line Manager (2-3 years)
  • Strong pharmacovigilance experience in a CRO
  • Must have experience working with clinical and post-marketed products
  • PSUR, DSUR, signal detection and risk management experience is essential
  • Strong case processing experience
  • Must be currently residing in the UK and have the right to work here

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


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.

Key Words: Pharmacovigilance/ Drug Safety / Pharma /PV / UK/Reading/Hartley/Surrey/Slough/Manager

Posted: 01/04/2019 | NPJ Ref: 233034
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