Senior Pharmacovigilance Scientist

4720092
  • Job type

    Contract
  • Location

    Hertfordshire
  • Working Pattern

    Full-time
  • Specialism

    Drug Safety And Pharmacovigilance
  • Industry

    Pharmaceuticals
  • Pay

    £30 - £48 p/h OUTSIDE IR35

Senior Pharmacovigilance Scientist - 12 month + contract - Hybrid - Welwyn Garden City - Outside IR35

Your new company

My client is a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people’s quality of life, specialising in Oncology, neurology, rare diseases, ophthalmology and immunology. There is an opportunity for a Senior Pharmacovigilance Scientist to join their Patient Safety Operations - Data Transformation team on an initial 12-month rolling contract.

OUTSIDE IR35
Hybrid -2 days in office per week

Your new role

As a highly motivated individual, you will use your pharmacovigilance expertise, particularly individual case safety report (ICSR) knowledge, to ensure safety data is processed and reported in a high-quality, compliant manner, so it can be used to understand and communicate the product benefit risk to protect patients’ safety.

  • Performing oversight of service providers who execute ICSR tasks (and Medical Device reports)
  • Answering queries and proactive sharing of your subject matter expertise to stakeholders (internally, at the service provider, business partners, auditors and inspectors)
  • Conducting process reviews to design and implement process improvements
  • Identifying root causes of non-compliance to agree Corrective Actions and Preventative Actions (CAPAs), which you may be responsible for implementing
  • Impact assessment of new / updated regulatory requirements

What you'll need to succeed

  • Life sciences degree
  • Proven Pharmacovigilance experience in the pharmaceutical industry - Demonstrated experience in a breadth of areas pertaining to pharmacovigilance, and pharmacovigilance legislation; good knowledge of international regulations (ICH, EU GVP Modules, FDA) and an understanding of the pharmaceutical industry (product development and the commercial environment) and of rapidly evolving personalised healthcare environment and ecosystem.
  • Medical Device processing experience, knowledge.
  • Evidence of leading complex, time-pressured projects, working with a wide range of stakeholders.
  • Evidence of proactive, self-driven, independent working

What you need to do now

Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK.

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

Apply for this job

Talk to Roberta Atkins, the specialist consultant managing this position

Located in London-City, 5th Floor, 107 Cheapside, Telephone 03330106292
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