Senior Pharmacovigilance Safety Data Transformation Lead


Company:	Hays Specialist Recruitment
Salary:	£29.85 to £48 an hour
Hours:	Full-time
Location:	Welwyn Garden City, EC2V 6DB
Working pattern:	Hybrid - 3 days remote
Job type:	Contract
Posting date:	9 Nov 2026
Closing date:	16 Nov 2026

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Summary

Your new company

Are you an experienced Pharmacovigilance professional looking to make a significant impact within a global, research-driven pharmaceutical organisation?

We are partnering with a leading international biopharmaceutical company to recruit a Senior Pharmacovigilance Safety Data Transformation Lead / Specialist within the Patient Safety Operations - Data Transformation team on a 12-month contract basis.

Within this team, you will use our 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 - having the biggest impact on patient safety.

Hybrid - 2 days Welwyn Garden City

OUTSIDE IR35

Ltd / Um - Up to £48 p/h

PAYE - Up to £35.82 p/h

Your new role

Key responsibilities include:

- Performing oversight of service provider who executes ICSR tasks (and Medical Device reports)

- Answering queries and proactive sharing of your subject matter expertise to stakeholders

- 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

We are keen to hear from experienced Pharmacovigilance professionals with a strong background in Pharmacovigilance within the pharmaceutical, biotechnology, or CRO sector.You will ideally possess:

- Significant pharmacovigilance and drug safety experience.

- 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).

- Desirable: 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.

This is a fantastic opportunity to join a world-class organisation at the forefront of healthcare innovation, working on cutting-edge therapies and contributing directly to patient safety on a global scale.Click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

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