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- 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.
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
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
Familiarise yourself with the latest pharmacovigilance regulations and guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the pharmacovigilance and clinical trial sectors. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends, which can give you an edge during discussions.
✨Tip Number 3
Prepare to discuss specific examples of your experience with safety data evaluation and risk assessments. Being able to articulate your past contributions will showcase your expertise and make you a more compelling candidate.
✨Tip Number 4
Research StudySmarter’s values and mission. Understanding our culture and how your role as a Global Patient Safety Scientist fits into our goals will help you align your answers during interviews 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 of a Global Patient Safety Scientist.
Craft a Compelling Cover Letter: In your cover letter, express your passion for patient safety and your understanding of global pharmacovigilance regulations. Mention how your background in biosciences equips you for this role and provide examples of your collaborative work with cross-functional teams.
Highlight Relevant Skills: Clearly outline your skills related to signal detection, risk assessment, and regulatory submissions. Use specific terminology from the job description to demonstrate your familiarity with the field and its requirements.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors and that your language is clear and professional. This reflects your attention to detail, which is crucial for the role.
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
This role requires working with various teams, so share examples of how you've successfully collaborated with regulatory, clinical development, or medical affairs teams in the past. Emphasise your communication skills and ability to work in a team environment.
✨Stay Updated on Regulatory Changes
Familiarise yourself with recent changes in global pharmacovigilance regulations. During the interview, mention any relevant updates you’ve followed and how they might impact safety surveillance practices.
✨Prepare for Technical Questions
Expect technical questions related to signal detection, risk assessments, and safety data handling. Brush up on your knowledge of these areas and be ready to explain your thought process when evaluating safety data.
