PV Specialist II | Remote (UK)
We’re partnering with a fast-growing CRO looking for a PV Specialist II to join their expanding pharmacovigilance team. This role is ideal for someone with previous case processing experience who wants to work across both clinical trial and post-marketing safety in a supportive, collaborative environment.
The Role
You’ll play a key part in day-to-day PV operations, including:
* Processing and entering a wide range of safety cases (AEs, SAEs, solicited reports, product complaints with AEs, med errors, pregnancies, follow-ups).
* Performing QC checks on cases completed by colleagues.
* Logging and triaging incoming reports from multiple channels, ensuring SAEs and priority cases are escalated quickly.
* Supporting database reconciliation activities with clinical and business partners.
* Maintaining accurate documentation and audit trails within the safety system.
* Monitoring shared PV inboxes and intake channels as part of the team rotation.
What You’ll Bring
* 3–5 years’ PV experience within pharma, biotech, or a CRO.
* Strong understanding of medical terminology and PV processes.
* Confidence using MedDRA, WHODrug, and safety systems (e.g., Argus, ARISg, Veeva Vault Safety).
* Exceptional attention to detail, strong organisational ability, and clear communication skills.
* Ability to work independently while contributing to a collaborative team.
Why Join?
* Fully remote role with UK-based flexibility.
* Opportunity to work across diverse therapy areas and case types.
* A growing company where progression is genuinely supported.
* A close-knit PV team that values quality, development, and teamwork.
If this sounds like the right next step, feel free to reach out for a confidential chat!