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For Companies At a Glance
- Tasks: Join our team as a Safety Scientist, overseeing drug safety from development to market.
- Company: Work with a leading global pharmaceutical company known for innovation and excellence.
- Benefits: Enjoy a hybrid work model with 2 days in North London and 3 days remote.
- Why this job: Make a real impact on patient safety while collaborating with top professionals in the field.
- Qualifications: Experience in signal detection and risk management is essential; strong analytical skills required.
- Other info: Opportunity to contribute to regulatory submissions and safety committees.
The predicted salary is between 43200 - 72000 £ per year.
Job Description
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.
As a Safety Scientist, you key responsibilities will include:
- 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
Hybrid: North London 2 days per week on site, 3 days remote
Applicants should have direct experience working with signal detection, aggregate reports and risk management plans in particular for both clinical and post-marketing activities.
Strong analytical, communication, and collaboration skills are essential for success in this role.
Associate Director Drug Safety Scientist employer: CPL
Contact Detail:
CPL Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director Drug Safety Scientist
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those working in drug safety and pharmacovigilance. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in safety science.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to drug safety and pharmacovigilance. This knowledge will not only enhance your understanding but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare to discuss specific examples of your experience with signal detection and risk management plans. Be ready to explain how you contributed to safety assessments and regulatory submissions in your previous roles.
✨Tip Number 4
Showcase your analytical and communication skills by preparing thoughtful questions for your interviewers. This will not only reflect your interest in the role but also your ability to engage in meaningful discussions about safety science.
We think you need these skills to ace Associate Director Drug Safety Scientist
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Associate Director Drug Safety Scientist position. Make sure you understand the key responsibilities and required skills, particularly around signal detection and risk management.
Tailor Your CV: Customise your CV to highlight relevant experience in safety science, pharmacovigilance, and any specific projects that demonstrate your analytical and communication skills. Use keywords from the job description to make your application stand out.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for drug safety and your understanding of the pharmaceutical industry. Mention specific experiences that relate to the responsibilities listed in the job description.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in the field of drug safety.
How to prepare for a job interview at CPL
✨Know Your Safety Science
Make sure you brush up on your knowledge of safety science principles, especially around signal detection and risk management plans. Be prepared to discuss your previous experiences in these areas and how they relate to the role.
✨Prepare for Technical Questions
Expect technical questions related to individual case safety reports (ICSRs) and aggregate reports like DSURs and PBRERs. Familiarise yourself with the regulatory submissions process and be ready to explain your contributions to past projects.
✨Showcase Your Collaboration Skills
This role requires strong collaboration with internal teams and external partners. Prepare examples that demonstrate your ability to work effectively in a team setting and how you've contributed to high-quality safety deliverables.
✨Ask Insightful Questions
At the end of the interview, ask questions that show your interest in the company and the role. Inquire about their current projects in safety science or how they approach risk-benefit assessments. This shows you're engaged and eager to contribute.
