Job Description

Associate Pharmacovigilance (PVG) Specialist
Watford
Entry level
43,000 - 72,000 £ / year (est.)
PCD330194

At a Glance

Tasks: Monitor safety reports and support patient safety initiatives in a collaborative team.

Benefits: Flexible working environment with opportunities for professional growth.
Why this job: Kickstart your career in pharmacovigilance and make a real impact on patient safety.
The organisation: Bachelor’s degree in Life Sciences or related field; attention to detail is key.
Other info: Join a passionate team and learn from experienced professionals.
The predicted salary is between 43,000 - 72,000 £ per year.
Job Title: Associate Pharmacovigilance (PVG) Specialist
Location: Hybrid based in Letchworth
Department: PVG Division
At the organisation, we are on a mission to support innovation in healthcare - and we are looking for an Associate Pharmacovigilance (PVG) Specialist to join our growing team. This role is ideal for someone looking to take their first step into pharmacovigilance or continue developing their experience in a supportive, collaborative environment. If you are detail-oriented, curious, and passionate about patient safety, this is an exciting opportunity to develop your skills and make an impact across global PV projects.
What will the role entail?
Monitor centralised PV mailboxes and other intake channels (e.g., fax, phone) for incoming safety reports
Perform initial review and intake of all safety information, including: spontaneous and solicited Adverse Events (AEs), serious Adverse Events (SAEs) from clinical trials and post-marketing sources, product Complaints (PCs) with associated AEs, medical inquiries, pregnancy reports, and medication errors, follow-up information for existing cases
Accurately log and create initial case records in the safety database in a timely and compliant manner
File and maintain all source documentation to ensure full audit traceability
Identify valid versus non-valid cases and route information to the appropriate departments in line with SOPs
Prioritise urgent and serious cases to support timely regulatory reporting
Support the Case Management Team with information sourcing and follow-up tasks
Assist with reconciliation activities and departmental metrics reporting

Why Join?

Work as part of a passionate, growing PV team focused on improving patient safety worldwide.
Enjoy a supportive, flexible environment with opportunities to learn from experienced PV professionals.
Be part of a company that values innovation, collaboration, and career growth.
Interested?
The organisation below or reach out to our recruitment team at to learn more about this opportunity.
At the organisation, we pride ourselves on being an excellent employer by fostering a supportive and collaborative work culture that prioritises employee growth and innovation in healthcare. As an Associate Pharmacovigilance (PVG) Specialist, you will benefit from a flexible hybrid working environment in Letchworth, where you can develop your skills alongside experienced professionals dedicated to improving patient safety globally. Join us to make a meaningful impact while enjoying opportunities for continuous learning and career advancement.

As you gain experience, you will have opportunities to:
Perform full case data entry for both serious and non-serious cases
Conduct quality control reviews of processed cases
Support safety data reconciliation with clinical databases and partners
Maintain departmental trackers and contribute to process improvements
What will you need to succeed?
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or another health-related field
Basic understanding of medical terminology and pharmacovigilance principles
Familiarity with safety databases (e.g., enterprise technology platform Argus, ARISg, Veeva Vault Safety) is a strong plus but not essential
Exceptional attention to detail and commitment to accuracy
Strong critical thinking and problem-solving abilities
Excellent organisational and time-management skills with the ability to meet deadlines
Clear and professional written and verbal communication
Proficiency in productivity suite (email application, word-processing application, spreadsheet application)
Ability to handle sensitive and confidential information with discretion