Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Ensure accuracy and compliance of pharmacovigilance reports while collaborating with diverse teams.
- Company: Join a leading global pharmaceutical company known for excellence and innovation.
- Benefits: Competitive salary, career growth opportunities, and a supportive work environment.
- Why this job: Make a real impact in drug safety and contribute to global health.
- Qualifications: Degree in a related field and 3+ years of experience in report authoring.
- Other info: Be part of an award-winning team that values diversity and inclusion.
The predicted salary is between 40000 - 50000 £ per year.
Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Pharmacovigilance Scientist to join the business in Slough.
Key Responsibilities:
- Perform quality control (QC) review of pharmacovigilance aggregate reports (e.g. PSURs/PBRERs, DSURs) to ensure accuracy, completeness, and compliance with regulatory requirements.
- Verify consistency of safety data, tables, listings, and narratives across multiple data sources.
- Ensure reports align with global regulatory guidelines and internal standard operating procedures.
- Identify discrepancies, errors, or data gaps and provide clear, actionable feedback to authors.
- Collaborate with cross-functional teams including safety scientists, medical writers, and data analysts to resolve QC findings.
- Support timelines by prioritising QC activities and ensuring on-time delivery of high-quality reports.
- Maintain documentation of QC activities, findings, and resolutions in accordance with compliance standards.
- Contribute to continuous improvement of QC processes, templates, and best practices.
- Assist in the preparation for audits and inspections by ensuring QC documentation is complete and inspection-ready.
- Support training and guidance for team members on QC standards and expectations where required.
Key Requirements:
- Degree in a related field (preferred).
- 3+ years experience authoring aggregate reports.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Pharmacovigilance Scientist in London employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmacovigilance Scientist in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory guidelines and QC processes. We recommend practising common interview questions with a friend to boost your confidence.
✨Tip Number 3
Showcase your skills! Bring along examples of your previous work, especially any aggregate reports you've authored. This will help you stand out and demonstrate your expertise.
✨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 Scientist in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Pharmacovigilance Scientist role. Highlight your experience with aggregate reports and quality control, as this will show us you’re a perfect fit for what we need.
Showcase Your Experience: Don’t just list your previous jobs; explain how your 3+ years of experience in authoring aggregate reports has prepared you for this role. We want to see specific examples that demonstrate your skills and achievements.
Be Clear and Concise: When writing your application, keep it straightforward and to the point. Use clear language and avoid jargon unless it’s relevant to the role. This helps us quickly understand your qualifications and fit for the position.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates regarding your application status.
How to prepare for a job interview at Planet Pharma
✨Know Your Reports Inside Out
Make sure you’re familiar with pharmacovigilance aggregate reports like PSURs and DSURs. Brush up on the regulatory requirements and internal SOPs, as being able to discuss these confidently will show your expertise and readiness for the role.
✨Prepare for Data Consistency Questions
Expect questions about how you verify the consistency of safety data across multiple sources. Have examples ready that demonstrate your attention to detail and problem-solving skills when identifying discrepancies or data gaps.
✨Showcase Your Collaboration Skills
Since the role involves working with cross-functional teams, be prepared to discuss your experience collaborating with safety scientists, medical writers, and data analysts. Highlight specific instances where your teamwork led to successful outcomes.
✨Emphasise Continuous Improvement
Talk about any initiatives you’ve taken to improve QC processes or templates in your previous roles. This shows that you’re proactive and committed to enhancing quality standards, which is crucial for this position.