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- Tasks: Oversee pharmacovigilance activities and ensure compliance with regulatory requirements.
- Company: Join a leading manufacturer of generic pharmaceuticals dedicated to enhancing daily healthcare.
- Benefits: Enjoy a hybrid work model with 3 days onsite in Surrey.
- Why this job: Be part of a mission-driven team focused on safety and regulatory excellence.
- Qualifications: Experience in pharmacovigilance and strong understanding of regulatory standards required.
- Other info: Collaborate with cross-functional teams and support the Medical Information team.
The predicted salary is between 48000 - 72000 £ per year.
Senior Pharmacovigilance (PV) Officer
I am working exclusively with a long standing client who are a global leader in pharmaceutical generics manufacturing. Due to a recent internal promotion, we are now looking to appoint a new Senior Pharmacovigilance (PV) Officer. The team also has immediate responsibility for scientific / medical information, although there is another member of the team that brings greater experience in this area. However, you will also be getting involved with scientific / medical information issues.
The role will be hybrid with up to two days remote work available but flexibility required.
Regulatory Knowledge: Experience in dealing with safety data exchange agreements and implementing risk minimization materials would be strong advantageous
PV, pharmacovigilance, information, scientific, medical, drug, safety, manufacturing, MHRA, advisor, generics
Senior Pharmacovigilance Officer employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Pharmacovigilance Officer
✨Tip Number 1
Familiarize yourself with the latest regulations and guidelines in pharmacovigilance. Understanding the current compliance landscape will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the pharmacovigilance field. Attend industry conferences or webinars to connect with others and gain insights into best practices, which can give you an edge during discussions with us.
✨Tip Number 3
Prepare to discuss specific examples of how you've managed Safety Data Exchange Agreements (SDEAs) or handled case management in your previous roles. Real-life scenarios can showcase your expertise and problem-solving skills.
✨Tip Number 4
Stay updated on recent developments in risk minimization measures and signal detection. Being knowledgeable about these topics will show us that you're proactive and ready to contribute to our mission from day one.
We think you need these skills to ace Senior Pharmacovigilance Officer
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly understand the responsibilities and requirements of the Senior Pharmacovigilance Officer position. Highlight your relevant experience in pharmacovigilance, compliance, and risk management in your application.
Tailor Your CV: Customize your CV to reflect your expertise in pharmacovigilance activities, such as managing Safety Data Exchange Agreements and signal detection. Use specific examples that demonstrate your ability to maintain audit readiness and enhance PV processes.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for pharmaceutical safety and regulatory standards. Mention how your skills align with the company's mission to support daily healthcare needs and your commitment to compliance.
Proofread Your Application: Before submitting, carefully proofread your application materials for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in the field of pharmacovigilance.
How to prepare for a job interview at RBW Consulting
✨Understand Pharmacovigilance Regulations
Make sure you are well-versed in the latest pharmacovigilance regulations and guidelines. Familiarize yourself with the specific requirements for the UK and ROI, as this will demonstrate your commitment to compliance and safety.
✨Showcase Your Experience with SDEAs
Be prepared to discuss your experience managing Safety Data Exchange Agreements (SDEAs). Highlight any specific challenges you've faced and how you successfully navigated them, as this is a key responsibility of the role.
✨Emphasize Cross-Functional Collaboration
This position requires collaboration across various teams. Share examples of how you've worked effectively with different departments, such as Medical Information or Quality Assurance, to enhance pharmacovigilance processes.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills in pharmacovigilance. Think about past experiences where you had to manage risk minimization measures or handle unsolicited inquiries, and be ready to explain your approach.
