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- Tasks: Manage pharmacovigilance activities and mentor team members in a dynamic environment.
- Company: Join Evestia Clinical, a leading global Clinical Research Organisation focused on innovative therapies.
- Benefits: Enjoy a supportive culture with opportunities for growth and development in your career.
- Why this job: Be part of a vital team impacting patient safety and drug development in exciting therapeutic areas.
- Qualifications: Degree in Pharmacy or Biological Science; experience in pharmacovigilance is essential.
- Other info: Flexible interview process with a recruiter and managers, plus a technical test.
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 of these platforms can set you apart during the interview process.
✨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 that demonstrate your attention to detail and ability to meet deadlines.
✨Tip Number 3
Since mentoring is a part of the role, think about instances where you've supported or guided team members in the past. Highlighting your leadership skills can show that you're a good fit for the team dynamic.
✨Tip Number 4
Research Evestia Clinical and their recent acquisition by Kester Capital. Understanding their goals and how you can contribute to their growth will help you make a strong impression during your interviews.
We think you need these skills to ace Pharmacovigilance (PVG) Associate II/ Senior PVG Associate
Some tips for your application 🫡
Understand the Role: Thoroughly read the job description for the Pharmacovigilance Associate II/Senior PVG Associate position. Make sure you understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience in pharmacovigilance and any relevant roles within a Clinical Research Organisation (CRO). Be specific about your previous responsibilities and achievements that align with the job requirements.
Showcase Your Skills: Mention any specific skills or tools you have experience with, such as MedDRA coding, Veeva, or other PV data systems. Highlight your ability to mentor others and your experience with regulatory submissions, as these are crucial for the role.
Craft a Compelling Cover Letter: Write a personalised cover letter that connects your background to Evestia Clinical's mission and values. Express your enthusiasm for the role and how you can contribute to the team, especially in areas like client communications and project support.
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 ensure quality control and effective case processing.
✨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 your previous roles. If not, do some research to understand their functionalities and importance in pharmacovigilance.
✨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 meetings or audits, and how you represent your team and project progress effectively.
