At a Glance
- Tasks: Support drug safety and compliance in a part-time role with flexible remote work.
- Company: IBSA UK, a leader in pharmacovigilance with a commitment to safety.
- Benefits: Gain valuable experience in the pharmaceutical industry while working remotely.
- Other info: Opportunity for professional growth and collaboration across diverse teams.
- Why this job: Make a real difference in drug safety and regulatory compliance.
- Qualifications: Degree in Life Sciences and 1-3 years of relevant experience required.
The predicted salary is between 24000 - 36000 € per year.
We are seeking a dedicated Pharmacovigilance Officer to provide essential drug safety support for IBSA UK. This part-time position plays a key role in maintaining compliance with UK regulatory standards and supporting the Local Person for Pharmacovigilance (LPPV).
You will act as the operational lead for UK pharmacovigilance activities, ensuring timely and accurate handling of safety data, maintaining documentation, and supporting inspection readiness. The role also includes occasional medical information responsibilities and collaboration across multiple teams.
Key Responsibilities- Assist the LPPV in ensuring the UK PV system meets MHRA and EU GVP requirements.
- Manage day-to-day safety operations, including adverse event intake, triage, and quality checks.
- Maintain PV documentation, agreements, and compliance records.
- Support audits, inspections, and risk management activities.
- Liaise with internal teams (Legal, QA, Clinical, Commercial) to embed PV obligations in contracts.
- Provide basic PV training to colleagues and partners.
- Respond to routine medical information queries and escalate complex cases appropriately.
- Degree in Life Sciences (Pharmacy, Pharmacology, Biomedical Sciences, Medicine, or similar).
- 1–3 years’ experience in pharmacovigilance or medical information (UK experience preferred).
- Knowledge of MHRA requirements, UK GVP Addendum, and EU GVP Modules.
- Familiarity with ABPI Code of Practice is advantageous.
- Strong organisational skills, attention to detail, and ability to work independently.
Drug Safety Officer in London employer: Actalent
IBSA UK is an excellent employer for those seeking a meaningful role in drug safety, offering a supportive work culture that prioritises compliance and collaboration. With flexible remote working arrangements and opportunities for professional growth, employees can thrive while contributing to vital pharmacovigilance activities. The company's commitment to employee development and its focus on maintaining high regulatory standards make it an attractive place for dedicated professionals in the life sciences field.
StudySmarter Expert Advice🤫
We think this is how you could land Drug Safety Officer in London
✨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 in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of MHRA and EU GVP requirements. We recommend creating a cheat sheet of key points to discuss, so you can impress your interviewers with your expertise.
✨Tip Number 3
Showcase your organisational skills! During interviews, share examples of how you've managed safety operations or documentation in the past. We want to see how you handle the nitty-gritty details that matter in this role.
✨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 are proactive about their job search.
We think you need these skills to ace Drug Safety Officer in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in pharmacovigilance and any specific skills that match the job description. We want to see how your background aligns with the role, so don’t be shy about showcasing your achievements!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about drug safety and how your experience makes you the perfect fit for our team. Keep it concise but engaging – we love a good story!
Showcase Your Knowledge:Since this role involves compliance with UK regulatory standards, make sure to mention your understanding of MHRA and EU GVP requirements. We appreciate candidates who are well-versed in the industry standards and can hit the ground running.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the easiest way for us to keep track of your application and ensures you get all the latest updates. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Actalent
✨Know Your Stuff
Make sure you brush up on your knowledge of pharmacovigilance and the specific regulations like MHRA and EU GVP. Being able to discuss these topics confidently will show that you're serious about the role and understand the industry's standards.
✨Showcase Your Experience
Prepare examples from your past work that highlight your experience in managing safety operations and handling adverse events. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.
✨Be Ready for Teamwork Questions
Since the role involves liaising with various internal teams, be prepared to discuss how you've collaborated with others in the past. Think of specific instances where your communication skills made a difference in achieving a common goal.
✨Ask Smart Questions
At the end of the interview, have a few thoughtful questions ready about the company's approach to pharmacovigilance or how they handle compliance challenges. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
