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Job Details
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Drug Safety Associate

Business Type: Pharmaceutical Company, Clinical Research Organisation, Contract Research Organisation
Job Type: Pharmacovigilance
Job Level: Experienced (non manager)
Position: Full Time
Location: London
Reference: NS78232
Closing Date: 23/04/20
Job Details:

Drug Safety Associate


Location: Central London

Salary: £Competitive plus benefits


An excellent Drug Safety Associate opportunity has come through with an expanding CRO specialising in a variety of therapeutic areas globally. The ideal candidate for this position should have strong previous industry experience and looking to develop and grow their career even further.


  • Working with the Clinical Safety Manager to ensure delivery of projects
  • Collecting, processing and tracking the Serious Adverse Event (SAE) reports
  • Generating study report narratives
  • Interacting with investigative sites based internationally, including Europe
  • Safety Surveillance duties
  • Oversight of the submission of safety reports in to Competent Authorities/Ethics Committees whilst complying with regulatory timelines
  • Data entry into the EudraVigilance portal
  • Interaction with internal and global departments such as Clinical Operations, Data Management and Regulatory Submissions
  • Drafting the study specific safety documents as required
  • Training and mentoring of team members


  • BSc in a relevant Science subject (Masters is an added bonus)
  • Relevant industry experience- 3 years plus
  • Experience working in Clinical Safety
  • Ability to work independently and in a team environment
  • Ability to manage own workload
  • Good IT skills- Microsoft Office
  • Excellent knowledge of GCP and Medical terminology
  • Knowledge of EDC and Safety databases
  • Ideally knowledge of safety reporting EU guidelines

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/London/Drug Safety/Clinical Safety/Pharmcovigilance/Clinical/PV Officer/

Posted: 26/03/2020 | NPJ Ref: 252371
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