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- Tasks: Monitor safety reports and support patient safety initiatives in a collaborative team.
- Company: Evestia Clinical, dedicated to innovation in healthcare.
- Benefits: Flexible working environment with opportunities for professional growth.
- Why this job: Make a real impact on global patient safety projects while developing your skills.
- Qualifications: 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 36000 - 60000 £ per year.
Associate Pharmacovigilance (PVG) Specialist
Job Title: Associate Pharmacovigilance (PVG) Specialist
Location: Hybrid based in Letchworth
Department: PVG Division
At Evestia Clinical, we’re on a mission to support innovation in healthcare – and we’re 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’re 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.
Overview
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
Opportunities as you gain experience
- 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., Oracle 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 Microsoft Office Suite (Outlook, Word, Excel)
- Ability to handle sensitive and confidential information with discretion
Why Join Us?
- 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?
Apply below or reach out to our recruitment team at rosalind@fusiongroupglobal.com to learn more about this opportunity.
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Associate Pharmacovigilance (PVG) Specialist employer: Evestia Clinical
Contact Detail:
Evestia Clinical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Pharmacovigilance (PVG) Specialist
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by researching common PVG scenarios and case studies. We recommend practising your responses to potential questions about patient safety and adverse events to show you're ready to dive in.
✨Tip Number 3
Show off your passion for patient safety! During interviews, share any relevant experiences or projects that highlight your commitment to this field. It’s all about demonstrating that you care.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team.
We think you need these skills to ace Associate Pharmacovigilance (PVG) Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Associate Pharmacovigilance role. Highlight any relevant experience or skills that match the job description, especially your attention to detail and understanding of medical terminology.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for patient safety and pharmacovigilance. Share specific examples of how your background aligns with the responsibilities outlined in the job description.
Showcase Your Skills: Don’t forget to mention your proficiency in Microsoft Office and any familiarity with safety databases. Even if you’re not an expert, showing a willingness to learn can set you apart from other candidates.
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 don’t miss out on any important updates about the role!
How to prepare for a job interview at Evestia Clinical
✨Know Your Stuff
Make sure you brush up on pharmacovigilance principles and medical terminology. Familiarity with safety databases like Oracle Argus or Veeva Vault Safety can give you an edge, even if it’s not essential. Show that you’re keen to learn and grow in this area!
✨Showcase Your Attention to Detail
As an Associate PVG Specialist, attention to detail is crucial. Prepare examples from your past experiences where your meticulous nature made a difference. This could be anything from academic projects to previous jobs—just make sure it highlights your ability to handle sensitive information accurately.
✨Communicate Clearly
Practice your verbal and written communication skills before the interview. You might be asked to explain complex concepts simply, so think about how you would describe pharmacovigilance to someone without a medical background. Clear communication is key in this role!
✨Be Ready for Scenario Questions
Expect questions that assess your critical thinking and problem-solving abilities. Think of scenarios related to patient safety or case management and how you would approach them. This will show your potential employer that you can handle the responsibilities of the role effectively.