Local QPPV – PharSafer® – Global Clinical and Post Marketing Drug Safety

Local QPPV

About the job

We are looking for experienced Local QPPVs to join our global team! This role is ideal for professionals with strong Pharmacovigilance (PV) experience, a passion for compliance, and the drive to make a global impact in drug safety.

PharSafer® is a specialist Pharmacovigilance & Medical Service CRO, headquartered in the UK with a worldwide client presence. We are an established Company having grown over the past 21 years.

Due to continued global growth, we are looking for Local QPPVs in various regions, including EU countries (e.g., France, Germany, Italy, Spain, Portugal, Poland, Belgium, Croatia), Switzerland, South America (e.g., Brazil, Mexico), Russia, Arab States (e.g. Dubai, Egypt, Saudi Arabia), Singapore, Japan, Turkey, and Africa (e.g., South Africa, Ghana).

As a Local QPPV, you will play a vital role in ensuring local Pharmacovigilance compliance, contributing to our mission to deliver the highest standards in drug safety and regulatory adherence. These roles are based in various global regions as listed above, with the flexibility of homeworking.

All local QPPVs will be linked to the Global PharSafer Headquarters and regular meetings will take place with the PharSafer QPPV Forum.

Responsibilities:

  • Demonstrate a strong working knowledge of local Pharmacovigilance and legislation, supporting local and global compliance activities.
  • Fulfil the role of Local QPPV, meeting and exceeding local PV regulations and requirements.
  • Provide regular updates on local legislation, with a focus on PV, regulatory affairs, and clinical developments.
  • Ensure full adherence to PharSafer’s Standard Operating Procedures (SOPs) and contribute to the maintenance of quality standards.
  • Have oversight of PV activities, including the collection, processing, and evaluation of adverse event reports, working in areas such as drug safety, medical devices, and cosmetics.
  • Act as a key contact for local PV queries, providing support to both internal and external stakeholders.
  • Contribute to the development of risk management plans and safety-related labelling changes.
  • Review local Periodic report submissions.
  • Support internal training and development, ensuring team members stay current with local and international PV regulations.
  • Participate in audits and inspections, contributing to audit/inspection readiness and continuous improvement.

Qualifications & Skills:

  • Bachelor’s or Master’s degree in Medicine, Pharmacy, Medical Science, or a related life science field.
  • Minimum of 5 years' experience in Pharmacovigilance, with exposure to PV processes, local regulatory requirements, and legislation.
  • Strong familiarity with PV databases, MedDRA coding, and regulatory platforms (e.g., Eudravigilance).
  • Excellent written and verbal communication skills in English and proficiency in the local language of the region.
  • Strong analytical and problem-solving skills with an eye for detail and the ability to manage multiple tasks effectively.
  • Ability to work independently, with initiative, and collaboratively as part of a wider team.
  • Experience with audit and inspection readiness is desirable, as is the capability to manage and mentor junior staff.

Apply Now

If you are interested in this opportunity, please submit your resume and a cover letter highlighting your experience and suitability for the role

*Please note that there will be several stages of the recruitment process. There may also be a test to determine your knowledge and understanding of the legislation.

**Due to the volume of responses anticipated, should you have not received a response to your application within 4 weeks then please assume your application has been unsuccessful on this occasion. PharSafer® regret that we are unable to provide individual feedback on applications made.

***Candidates who do not match the specific requirements will also not be considered for interview for this position.

This is a career opportunity, not a job opportunity.

We look forward to hearing from you!

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