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For Companies At a Glance
- Tasks: Join our team to ensure patient safety through data analysis and regulatory compliance.
- Company: Be part of a global leader in healthcare dedicated to improving patient outcomes.
- Benefits: Enjoy flexible working options, professional development opportunities, and a collaborative culture.
- Why this job: Make a real impact on patient safety while working with diverse teams and innovative projects.
- Qualifications: A degree in biosciences and fluency in English are essential; experience in pharmacovigilance is a plus.
- Other info: Ideal for those passionate about science and making a difference in healthcare.
The predicted salary is between 36000 - 60000 £ per year.
Overview
We are seeking a scientifically driven and highly organized Safety Scientist to join a Global Patient Safety (GPS) team. This role plays a critical part in supporting the safety surveillance of clinical and post-marketing programs, contributing to signal management, regulatory documentation, and cross-functional collaboration. You’ll work across all phases of development, supporting safety data evaluation, risk assessments, and compliance with international pharmacovigilance regulations.
Responsibilities
- Conduct scientific review of safety data for aggregate reports (e.g., DSURs, PSURs, RMPs)
- Perform signal detection, evaluation, and risk assessment activities
- Support safety surveillance throughout clinical trials (Phases I–IV), including review of SAEs, AESIs, TEAEs
- Provide input into protocols, study reports, and clinical safety documentation
- Collaborate with cross-functional teams (Regulatory, Clinical Development, Medical Affairs, QA, etc.)
- Contribute to responses for health authority inquiries and safety-related submissions
- Liaise with vendors, CROs, and partners to ensure accurate, timely safety data handling
- Ensure SAE reconciliation between safety databases and clinical trial systems
- Monitor and interpret global pharmacovigilance regulatory changes and contribute to SOP updates
- Support safety oversight for Market Research and Patient Support Programs
Key Requirements
- Degree in a bioscience-related field (BSc, PharmD, MD)
- Fluency in English (written and spoken)
- Awareness of global pre- and post-marketing PV legislation
- Experience preparing or contributing to DSURs, PSURs, RMPs, or safety responses
- Understanding of pharmacovigilance responsibilities in clinical trials and post-marketing settings
- Familiarity with safety data related to organ toxicities is a plus
- Experience with regulatory submissions (NDA/BLA) or work within a regulatory agency is advantageous
Global Patient Safety Scientist employer: Meet Life Sciences
Contact Detail:
Meet Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Patient Safety Scientist
✨Tip Number 1
Network with professionals in the pharmacovigilance field. Attend industry conferences or webinars to meet people who work in global patient safety. This can help you gain insights into the role and potentially get referrals.
✨Tip Number 2
Stay updated on the latest regulations and guidelines in pharmacovigilance. Familiarise yourself with recent changes in global legislation, as this knowledge will be crucial during interviews and discussions with potential employers.
✨Tip Number 3
Prepare to discuss your experience with safety data evaluation and risk assessments. Be ready to provide examples of how you've contributed to safety surveillance in previous roles, as this will demonstrate your capability for the position.
✨Tip Number 4
Research StudySmarter's values and mission. Understanding our company culture and how we approach patient safety can help you tailor your conversations and show that you're a great fit for our team.
We think you need these skills to ace Global Patient Safety Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in pharmacovigilance and safety data evaluation. Emphasise any specific projects or roles that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: In your cover letter, express your passion for patient safety and your understanding of global pharmacovigilance regulations. Mention specific experiences that demonstrate your ability to conduct scientific reviews and collaborate with cross-functional teams.
Highlight Relevant Skills: Clearly outline your skills related to signal detection, risk assessment, and regulatory submissions. Use examples from your past work to illustrate how you have successfully managed safety data and contributed to safety documentation.
Proofread Your Application: Before submitting, carefully proofread your application materials for any errors or inconsistencies. A well-presented application reflects your attention to detail, which is crucial for a role in patient safety.
How to prepare for a job interview at Meet Life Sciences
✨Showcase Your Scientific Knowledge
Make sure to highlight your understanding of pharmacovigilance and safety data evaluation. Be prepared to discuss specific experiences where you've conducted scientific reviews or contributed to safety reports like DSURs or PSURs.
✨Demonstrate Cross-Functional Collaboration
Since this role involves working with various teams, share examples of how you've successfully collaborated with different departments. Emphasise your communication skills and ability to work in a team environment.
✨Stay Updated on Regulatory Changes
Familiarise yourself with the latest global pharmacovigilance regulations. During the interview, mention any recent changes you've monitored and how they could impact safety surveillance practices.
✨Prepare for Technical Questions
Expect questions related to risk assessments and signal detection. Brush up on your technical knowledge and be ready to explain your thought process when evaluating safety data or handling adverse events.
