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- Tasks: Support safety activities and conduct signal detection in clinical development.
- Company: Join a world-renowned global pharmaceutical company with a focus on safety science.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on patient safety and contribute to innovative healthcare solutions.
- Qualifications: Experience in signal detection and strong analytical skills required.
- Other info: Collaborative environment with opportunities to work with top professionals in the field.
The predicted salary is between 36000 - 60000 £ per year.
CPL Life Sciences are in collaboration with a world-renowned global pharmaceutical company who are seeking two new professionals at varying experience levels to join their Safety Science and Pharmacovigilance team. This role provides scientific safety oversight across the full lifecycle of investigational and marketed products.
Responsibilities
- Support safety activities in early and late-phase clinical development
- Conduct signal detection, evaluation, and contribute to risk‑benefit assessments
- Manage individual case safety reports (ICSRs) and prepare aggregate reports (e.g., DSURs, PBRERs)
- Participate in the preparation and review of regulatory submissions (INDs, NDAs, MAAs, etc.)
- Contribute to the development and maintenance of safety labeling and core safety documents
- Collaborate with internal teams and external partners to ensure high‑quality safety deliverables
- Provide safety input to study teams and participate in cross‑functional meetings
- Help prepare materials for safety committees (e.g., iDMCs, IMCs) and regulatory authorities
Working Conditions
Hybrid: North London 2 days per week on site, 3 days remote
Qualifications
Direct experience working with signal detection, aggregate reports and risk‑management plans for both clinical and post‑marketing activities. Strong analytical, communication and collaboration skills.
Associate Director Pharmacovigilance Scientist in London employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director 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. 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 signal detection and risk management plans. 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 from your past experiences where you contributed to safety assessments or regulatory submissions. We want to see how you can bring value to the team!
✨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 Associate Director Pharmacovigilance Scientist in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your direct experience with signal detection and aggregate reports, as these are key for the role.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about pharmacovigilance. Share specific examples of how you've contributed to safety activities in previous roles, and don’t forget to mention your collaboration skills!
Showcase Your Analytical Skills: Since strong analytical skills are crucial for this position, consider including a brief section in your application that demonstrates how you've successfully tackled complex problems in the past, especially related to risk management.
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’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Pharmacovigilance Basics
Make sure you brush up on your knowledge of signal detection, risk management plans, and aggregate reports. Being able to discuss these topics confidently will show that you understand the core responsibilities of the role.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific safety scenarios or case reports. Think about past experiences where you've had to evaluate risks or collaborate with teams, and be ready to share those examples.
✨Familiarise Yourself with Regulatory Submissions
Since the role involves preparing regulatory submissions, it’s crucial to know the ins and outs of INDs, NDAs, and MAAs. Research recent changes in regulations and be prepared to discuss how they might impact safety assessments.
✨Showcase Your Collaboration Skills
This position requires working closely with various teams. Be ready to talk about how you've successfully collaborated in the past, whether it's with internal teams or external partners, and highlight your communication skills.
