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For Companies At a Glance
- Tasks: Join our team to manage pharmacovigilance activities and mentor others.
- Company: Evestia Clinical is a global leader in clinical research, specialising in tailored trial services.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and mentorship.
- Why this job: Be part of a vital team impacting patient safety in innovative therapies.
- Qualifications: Degree in Pharmacy or Biological Science; PVG experience required.
- Other info: Exciting opportunity to grow with a newly independent company post-acquisition.
The predicted salary is between 36000 - 60000 £ per year.
Evestia Clinical is a specialised, full-service global Clinical Research Organisation that offers market-leading experience and expertise to pharmaceutical and biotech companies. Evestia Clinical provides bespoke and tailored clinical trial services across therapeutic areas including oncology, rare disease, inflammation, immunology and microbiome therapeutics.
The Role
We are looking for a Pharmacovigilance Associate II/ Senior Pharmacovigilance Associate, level determined on years of experience, to join the PVG team within the Clinical Development Division of Evestia Clinical.
What will it entail?
- Perform and oversee pharmacovigilance case management activities, including case triage, data entry, MedDRA coding, follow-ups, and regulatory submissions.
- Mentor and support Case Management Team members, including providing guidance on quality control and case processing tasks.
- Participate in client communications, meetings, and audits, representing the Case Management Team and project progress.
- Assist in the development and maintenance of pharmacovigilance systems, SOPs, and work instructions for both Evestia Clinical and clients.
- Ensure high levels of accuracy and compliance with deadlines, SOPs, and regulatory standards in all tasks performed.
- Support Project Leaders with broader PVG activities, including PSURs, RMPs, and PSMFs as required.
- Utilise PV data systems (e.g., eVigi, eSafety, Veeva) for case processing and documentation tracking.
- Contribute to invoicing processes and support project financials when requested.
- Ensure proper documentation, reconciliation, and archiving of case files and communications.
- Provide backup support to Pharmacovigilance Assistants and Leads as needed, ensuring team continuity and workflow coverage.
What will you need?
- Educated to degree level in Pharmacy, Biological Science or similar.
- Experience within a CRO environment would be advantageous.
- Experience working with small biotech companies would be advantageous.
- Previous experience in PVG & safety is essential. Depending on the number of years the role will either be PVG II or Senior PVG Associate.
- Experience within VeeVa would be advantageous.
What will the Interview Process be?
An initial call with the recruiter Sarah Nedjai, followed by a 30 minute call with the managers, finished by a technical test.
If you would like to be part of a growing & evolving team then please apply to the role! Best of luck 😊
Pharmacovigilance (PVG) Associate II/ Senior PVG Associate employer: Evestia Clinical
Contact Detail:
Evestia Clinical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance (PVG) Associate II/ Senior PVG Associate
✨Tip Number 1
Familiarise yourself with the specific pharmacovigilance systems mentioned in the job description, such as eVigi, eSafety, and Veeva. Having a solid understanding of these tools will not only boost your confidence but also demonstrate your readiness to hit the ground running.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of MedDRA coding and regulatory submissions. Being able to discuss these topics fluently will show that you are well-versed in the essential aspects of the role.
✨Tip Number 3
Highlight any mentoring or leadership experience you have during the interview. Since the role involves supporting and guiding team members, showcasing your ability to lead will make you a more attractive candidate.
✨Tip Number 4
Research Evestia Clinical and its recent acquisition by Kester Capital. Understanding the company's direction and growth plans will allow you to tailor your responses and show genuine interest in being part of their evolving team.
We think you need these skills to ace Pharmacovigilance (PVG) Associate II/ Senior PVG Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in pharmacovigilance and any specific skills related to case management, regulatory submissions, and the use of PV data systems like Veeva. Customise your CV to reflect the requirements mentioned in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmacovigilance and your understanding of the role at Evestia Clinical. Mention your educational background, relevant experience, and how you can contribute to the team. Be sure to express your enthusiasm for joining a growing and evolving team.
Highlight Relevant Experience: In your application, emphasise any previous roles in pharmacovigilance or within a CRO environment. If you have experience with small biotech companies or specific tools like eVigi or eSafety, make sure to include that as well.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Ensure that your application is clear, concise, and professional, as attention to detail is crucial in the pharmacovigilance field.
How to prepare for a job interview at Evestia Clinical
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your pharmacovigilance knowledge, especially case management activities. Be prepared to discuss your experience with MedDRA coding and regulatory submissions, as these are crucial for the role.
✨Showcase Your Mentoring Skills
Since the role involves mentoring team members, think of examples where you've supported or guided others in a professional setting. Highlight your ability to provide constructive feedback and ensure quality control.
✨Familiarise Yourself with Relevant Systems
If you have experience with PV data systems like eVigi, eSafety, or Veeva, be ready to discuss how you've used them in past roles. If you're not familiar with these systems, do some research to understand their functionalities.
✨Prepare for Client Interaction Scenarios
As client communication is part of the job, think about how you would handle various scenarios. Prepare to discuss your experience in client meetings and audits, and how you represent your team effectively.
