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For Companies At a Glance
- Tasks: Process safety cases and support pharmacovigilance operations in a collaborative team.
- Company: Fast-growing CRO with a supportive and dynamic work culture.
- Benefits: Fully remote role, flexible hours, and genuine career progression opportunities.
- Why this job: Join a close-knit team and make a real impact in patient safety.
- Qualifications: 3-5 years of pharmacovigilance experience and strong medical terminology knowledge.
- Other info: Work across diverse therapy areas and enhance your professional skills.
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!
Pharmacovigilance Specialist II in Lincoln employer: Fusion Group
Contact Detail:
Fusion Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance Specialist II in Lincoln
✨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. Be ready to discuss your previous case processing experience and how it relates to the role of a PV Specialist II.
✨Tip Number 3
Show off your attention to detail! During interviews, share examples of how you've maintained accurate documentation and performed QC checks. This will demonstrate your fit for the role and your commitment to quality.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Pharmacovigilance Specialist II in Lincoln
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: Since this role requires exceptional attention to detail, make sure your application is free from typos and errors. We appreciate candidates who take the time to double-check their work, so let that shine through in your written application!
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 keen on joining our team at StudySmarter!
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 as the specific safety systems mentioned in the job description. This will show that you're not just interested but also knowledgeable about 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. Highlight any situations where you had to escalate cases quickly or manage incoming reports, as this will demonstrate your ability to handle the responsibilities of the role.
✨Emphasise Teamwork
Since this role involves collaboration, be ready to talk about how you work within a team. Share examples of how you've contributed to a supportive environment in past roles, and how you balance independent work with teamwork. This will resonate well with the company's values.
✨Ask Smart Questions
Prepare thoughtful questions to ask at the end of your interview. Inquire about the team dynamics, ongoing projects, or how they support professional development. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.