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- 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.
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!
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 hands-on experience or knowledge about these platforms can give you a significant edge during the interview.
✨Tip Number 2
Prepare to discuss your previous experiences in case management and how you've ensured compliance with regulatory standards. Be ready to provide examples of how you've mentored team members or improved processes in your past roles.
✨Tip Number 3
Research Evestia Clinical and their recent acquisition by Kester Capital. Understanding their vision and how they plan to grow as an independent business will help you align your answers with their goals during the interview.
✨Tip Number 4
Practice articulating your knowledge of pharmacovigilance regulations and guidelines. Being able to confidently discuss these topics will demonstrate your expertise and commitment to the role, making you a more attractive candidate.
We think you need these skills to ace Pharmacovigilance (PVG) Associate II/ Senior PVG Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Pharmacovigilance Associate II/Senior PVG Associate position. Understand the key responsibilities and required qualifications to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience in pharmacovigilance, particularly within a CRO environment or with small biotech companies. Mention specific tasks you've performed that align with the job requirements, such as case management activities or regulatory submissions.
Showcase Your Skills: Make sure to highlight your skills related to data entry, MedDRA coding, and familiarity with PV data systems like Veeva. Providing examples of how you've used these skills in past roles can strengthen your application.
Craft a Strong Cover Letter: Write a compelling cover letter that not only outlines your qualifications but also expresses your enthusiasm for joining Evestia Clinical. Mention your interest in contributing to their growth and how your background aligns with their mission.
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 leadership qualities and how you can contribute to team development.
✨Familiarise Yourself with Relevant Systems
If you have experience with PV data systems like eVigi, eSafety, or Veeva, be ready to discuss it. If not, do some research on these systems to show your willingness to learn and adapt.
✨Prepare for Client Interaction Scenarios
As client communication is part of the job, prepare for questions about how you would handle client meetings or audits. Think of past experiences where you successfully managed client relationships or project progress.
