Senior Pharmacovigilance Officer - Risk Management

7 days left

Essex + remote working
Competitive salary and benefits
24 Apr 2021
24 May 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)


  • Full-time permanent position
  • Office based in Essex and some remote working
  • Competitive package



  • Preparation, review and submission of Aggregate Reports (PSUR/ DSUR/ PADER/ ACO)
  • Authoring/ updating of RMPs
  • Creation/ maintenance of CCDSs and creation of supporting documentation (CO, CES, etc.)
  • Assistance with compilation of safety variations, if required
  • Assisting with responding to regulatory authority queries
  • Compilation and presentation of submission metrics for aggregate reports
  • Authoring of signal assessment reports
  • Assisting with scheduling and forecasting of aggregate reports and signal management activities

Full job description available on application



  • Life science degree
  • Minimum 3 years in PV
  • A thorough foundation in pharmacovigilance, ideally having experience in various aspects of pharmacovigilance
  • Significant experience in authoring and reviewing aggregate reports, including PSURs, PADERs, DSURs, ACOs in line with applicable templates and guidance
  • Experience in authoring and updating RMPs in line with applicable template and guidelines


  • Only candidates with existing right to work in the UK/EU will be considered


Please complete the details below to apply. For further information or a discreet discussion regarding your recruitment requirements, please call Alex on 01227 844466 or email

To view our other vacancies, please visit our website on

Apex Recruitment are a specialist agency providing opportunities within the pharmaceutical, biopharma, biotech and medical device industries recruiting in the areas of medical affairs, drug safety, clinical and quality.

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