At a Glance
- Tasks: Join a dynamic team to process safety cases and ensure quality in pharmacovigilance.
- Company: Fast-growing CRO with a supportive and collaborative culture.
- Benefits: Fully remote role, flexible hours, and genuine career progression opportunities.
- Other info: Close-knit team that values quality, development, and teamwork.
- Why this job: Make a real impact in patient safety while working with diverse therapy areas.
- Qualifications: 3-5 years of PV experience and strong understanding of medical terminology.
The predicted salary is between 36000 - 60000 € per year.
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
- 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!
Locations
Pharmacovigilance Specialist II in Cheshire, Warrington employer: Fusion Group
Join a dynamic and rapidly expanding CRO as a Pharmacovigilance Specialist II, where you will thrive in a fully remote role that offers UK-based flexibility. Our supportive and collaborative work culture prioritises employee growth, providing opportunities to engage with diverse therapy areas while being part of a close-knit team that values quality and development. Experience meaningful work in an environment that genuinely supports your career progression.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmacovigilance Specialist II in Cheshire, Warrington
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmacovigilance field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for those interviews! Brush up on your knowledge of MedDRA, WHODrug, and safety systems. Being able to confidently discuss your experience with these tools will set you apart from the competition.
✨Tip Number 3
Showcase your attention to detail! During interviews, share specific examples of how you've maintained accurate documentation and performed QC checks. This will demonstrate your fit for the role and the importance of quality in pharmacovigilance.
✨Tip Number 4
Don’t forget to apply through our website! We’re always looking for talented individuals like you to join our growing team. Plus, it’s a great way to ensure your application gets the attention it deserves.
We think you need these skills to ace Pharmacovigilance Specialist II in Cheshire, Warrington
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Pharmacovigilance Specialist II role. Highlight your relevant experience in case processing and any specific systems you've used, like Argus or Veeva Vault Safety. We want to see how your background fits with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about pharmacovigilance and how your skills align with our needs. Keep it concise but engaging – we love a good story that showcases your journey in the field.
Showcase Your Attention to Detail:In pharmacovigilance, attention to detail is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their application is polished and professional!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re proactive and keen to join our team!
How to prepare for a job interview at Fusion Group
✨Know Your Stuff
Make sure you brush up on your pharmacovigilance knowledge, especially around case processing and medical terminology. Familiarise yourself with MedDRA and WHODrug as well, since these are crucial for the role.
✨Showcase Your Experience
Prepare to discuss your previous PV experience in detail. Think of specific examples where you've processed safety cases or performed QC checks. This will help demonstrate your hands-on expertise and how it aligns with what they’re looking for.
✨Be Ready for Teamwork Questions
Since this role involves collaboration, be prepared to talk about how you work within a team. Share examples of how you've contributed to team success or handled conflicts, showing that you can thrive in a supportive environment.
✨Ask Smart Questions
At the end of the interview, don’t forget to ask insightful questions about the company culture or the specific challenges the PV team is facing. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
