Senior Pharmacovigilance Scientist Job in London

Hendre Moolman at CK Clinical is currently recruiting for a Senior Pharmacovigilance Scientist to join a Pharmaceutical company based in London. This is a 12 month contract position.

Senior Pharmacovigilance Scientist Job Description

As Senior Pharmacovigilance Scientist, your primary objective will be to contribute and assist in EU QPPV pharmacovigilance activities, including PV system and processes oversight, compliance and Detailed Description of Pharmacovigilance Systems (DDPS). You will be representing the EU QPPV office and PV department internally and externally at a global level.

As Senior Pharmacovgilance Scientist, your key responsibilities will include:

  • Ensure that the EU QPPV has adequate oversight of the PV system including processes
  • Document the EU QPPV oversight of the PV system and its performance
  • Manage the Detailed Description of Pharmacovigilance Systems (DDPS) for updating and regulatory submissions
  • Maintain documentation necessary for EU QPPV office: mailbox, website, folders to ensure appropriate availability, and cross communication with all members of PV system
  • Review and carrying out and impact analysis (also solution proposals) on Health Authority proposals for changes in global pharmacovigilance regulations and guidelines
  • Collaborate with the Compliance Office in monitoring performance/compliance, training and receiving/distributing information as needed
  • Collaborate with the Compliance Office in Health Authority Inspections and internal audits
  • Contribute to SOP/SDEA review and writing
  • Contribute to improvement of departmental processes

As Senior Pharmacovigilance Scientist you will have the following qualifications, skills and experience:

  • Registered nurse or degree level qualification (e.g. Bachelors degree) in scientific/medical field
  • Proven experience in post marketing Pharmacovigilance plus any clinical experience
  • Experience with safety databases including simple searches & coding dictionaries (MedDRA)
  • Sound knowledge of clinical trial methodology and pharmacovigilance regulations (clinical and post marketing)
  • Ability to review, analyse, interpret and present data
  • Good level of computer literacy with Microsoft applications
  • Good organisation skills and ability to prioritise
  • Good communication and writing skills
  • Accuracy and attention to detail
  • Highly motivated and flexible
  • Ability to work in a team/matrix environment

How to apply:

Click here to apply online now.

To find out more about this Senior Pharmacovigilance Scientist position, please contact Hendre Moolman on 01438 870 023 or email  Please quote reference CL23472 in all correspondence.

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