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Senior Pharmacovigilance Scientist

CK Group- Science, Clinical and Technical

Welwyn Garden City
Vor Ort
GBP 80.000 - 100.000
Vor 27 Tagen
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Senior Pharmacovigilance Scientist
CK Group- Science, Clinical and Technical
Welwyn Garden City
Vor Ort
GBP 80.000 - 100.000
Vollzeit
Vor 27 Tagen

Zusammenfassung

A leading biopharmaceutical company is seeking a Senior Pharmacovigilance Scientist in Welwyn Garden City. This hybrid role requires expertise in pharmacovigilance and oversight of safety data processes. The ideal candidate has a relevant Life Science degree and experience in managing complex projects in a fast-paced environment. This contract position offers competitive hourly rates and requires 2 days per week onsite work.

Qualifikationen

  • Demonstrated experience in pharmacovigilance and relevant legislation.
  • Medical Device processing experience preferred.
  • Strong knowledge across end-to-end ICSR processes.

Aufgaben

  • Ensure high quality, compliant processing of safety data.
  • Oversee service providers executing ICSR tasks.
  • Lead complex initiatives with multiple stakeholders.

Kenntnisse

Pharmacovigilance expertise
Knowledge of international regulations
Project management
Problem-solving

Ausbildung

Relevant Life Science degree or equivalent experience
Jobbeschreibung
Overview

CK Group are recruiting for a Senior Pharmacovigilance Scientist to join a company in the pharmaceutical industry on an outside IR25 contract basis until the end of 2026.

Salary: £40 - £48 per hour UMB / LTD or £29.85 - £35.82 per hour PAYE

Location: Welwyn Garden City (Hybrid role, 2 days per week required on site).

Responsibilities
  • Use 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.
  • Perform oversigh t of service providers who execute ICSR tasks (and Medical Device reports).
  • Identify root causes of non-compliance to agree Corrective Actions and Preventative Actions (CAPAs), which you may be responsible for implementing.
  • Provide effective oversight of service providers via relationship management, and metrics and analysis.
  • Lead complex initiatives with multiple stakeholders, with the ability to investigate and creatively solve problems and simplify, whilst meeting customer needs.
Background / Qualifications
  • 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.
  • A relevant Life Science degree or equivalent experience in pharmacovigilance.
  • Strong broad knowledge across end-to-end ICSR processes.
Company

Our client is one of the world\'s premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Location

This role is based at our client\'s site in Welwyn Garden City (Hybrid role, 2 days per week required on site).

Apply

For more information, or to apply for this Senior Pharmacovigilance Scientist role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).

Other notes: It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

INDKA

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