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For Companies At a Glance
- Tasks: Monitor and assess medicine safety, manage adverse event reports, and ensure compliance.
- Company: Fast-growing pharmaceutical company focused on high-quality medicines.
- Benefits: Hybrid work, career growth opportunities, and impact on public health.
- Why this job: Make a real difference in patient safety while gaining valuable regulatory expertise.
- Qualifications: Degree in pharmacy or life sciences; experience in pharmacovigilance is a plus.
- Other info: Collaborate with diverse teams and enjoy a dynamic work environment.
The predicted salary is between 36000 - 60000 £ per year.
Smart4 Sciences is partnering with a fast-growing pharmaceutical company that develops and commercializes a wide portfolio of branded and generic medicines. They deliver high-quality products while building long-term partnerships across the value chain. We are now recruiting a Pharmacovigilance Officer to play a key role in supporting safety and compliance activities.
The Role
As Pharmacovigilance Officer, you will be responsible for a broad range of PV activities, including processing and training on Individual Case Safety Reports (ICSRs), liaising with regulators, identifying safety trends, and preparing case summaries and causality assessments. You will also review, draft, and approve PV documentation to ensure compliance with global standards.
Key Responsibilities
- Monitor, assess, and ensure the safety of medicines by managing adverse event reports.
- Collect, review, and process ADRs from healthcare professionals, patients, and literature.
- Enter cases into safety databases and ensure timely reporting to regulatory authorities.
- Identify potential safety signals and contribute to risk management plans.
- Maintain PV documentation systems and support preparation of narratives, case reports, and regulatory filings.
- Collaborate with clinical, regulatory, and medical affairs teams.
- Liaise with external partners, CROs, and regulatory agencies.
Desirable Skills & Experience
- Degree in pharmacy, life sciences, medicine, or related field (advanced qualifications such as MSc/PhD are advantageous).
- Knowledge of pharmacovigilance regulations (ICH, GVP, EMA, FDA).
- Experience with safety databases (e.g., Argus, ARISg, VigiBase).
- Strong analytical and data interpretation skills.
- Excellent attention to detail and accuracy in documentation.
- Effective communication skills for liaising with regulators and stakeholders.
- Ability to work under pressure and meet strict deadlines.
- Prior experience in pharmacovigilance, regulatory affairs, or clinical research.
- Familiarity with adverse event reporting and case processing.
Why Apply?
- Opportunity to work hybrid.
- Impact on Patient Safety - Play a vital role in protecting public health by monitoring and evaluating adverse drug reactions.
- Regulatory & Scientific Expertise - Gain deep knowledge of global regulations while sharpening analytical and scientific skills.
- Career Growth & Stability - PV is a rapidly expanding field with strong demand and clear progression opportunities into senior PV, regulatory affairs, or medical affairs roles.
- Cross-Functional Exposure - Collaborate with diverse teams across clinical research, regulatory affairs, medical information, and quality assurance.
To apply or find out more, contact for a confidential discussion.
Pharmacovigilance Officer in Coventry employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance Officer in Coventry
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be when it comes to landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of pharmacovigilance regulations and safety databases. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your analytical skills! During interviews, be ready to discuss specific examples where you identified safety trends or managed adverse event reports. We want to see how you think and solve problems in real-time.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Pharmacovigilance Officer in Coventry
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Pharmacovigilance Officer role. Highlight relevant experience, especially in pharmacovigilance regulations and safety databases. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about patient safety and how your background makes you a great fit for our team. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail: As a Pharmacovigilance Officer, attention to detail is key. In your application, make sure to demonstrate this skill. Whether it's through your CV formatting or the clarity of your writing, we want to see that you can handle the nitty-gritty!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team!
How to prepare for a job interview at Smart4Sciences
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your knowledge of pharmacovigilance regulations like ICH, GVP, EMA, and FDA. Being able to discuss these confidently will show that you’re serious about the role and understand the compliance landscape.
✨Showcase Your Analytical Skills
Prepare examples from your past experiences where you successfully identified safety signals or managed adverse event reports. Highlighting your analytical prowess will demonstrate your capability to handle the responsibilities of a Pharmacovigilance Officer.
✨Familiarise Yourself with Safety Databases
If you have experience with safety databases like Argus or ARISg, be ready to discuss it. If not, do some research on how these systems work and be prepared to explain how you would approach learning them quickly.
✨Practice Effective Communication
Since liaising with regulators and stakeholders is key in this role, practice articulating your thoughts clearly and concisely. You might even want to role-play potential scenarios to boost your confidence in communicating complex information.
