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For Companies At a Glance
- Tasks: Lead patient safety initiatives and assess risks for innovative medicines.
- Company: Join UCB, a global biopharmaceutical leader in neurology and immunology.
- Benefits: Inclusive culture, career growth, and the chance to make a real impact.
- Why this job: Be part of a team that prioritises patient safety and drives drug development.
- Qualifications: MD required; experience in pharmacovigilance and strong project management skills.
- Other info: Collaborative environment with diverse teams and a commitment to ethical decision-making.
The predicted salary is between 36000 - 60000 £ per year.
Are you passionate about advancing patient safety and drug development? Join our Brussels office in Belgium or Slough office in the UK.
About the Role
You will be working in a team that leads the strategic planning, delivery, and communication of benefit-risk assessments and risk management strategies for our medicines. Your focus will be on supporting clinical development from a safety perspective, identifying and assessing emerging safety concerns, evaluating benefit-risk outcomes, and supporting the implementation of risk management strategies that improve patient outcomes globally.
Who You’ll Work With
You will be collaborating in a diverse, cross-functional team, including experts in clinical development, regulatory affairs, patient engagement, medical affairs, and other stakeholders across the organization. The team values open communication, shared decision-making, and a commitment to patient safety.
What You’ll Do
- Analyze and interpret data from multiple sources to identify and assess potential new risks for assigned medicines.
- Incorporate new data into benefit-risk assessment plans.
- Implement safety monitoring and risk management strategies within clinical development programs.
- Identify areas requiring evidence generation, such as patient insights or real-world data, to support benefit-risk assessment plans.
- Serve as project manager, author, and reviewer of documents for regulatory submissions, ensuring clarity and compliance.
- Collaborate with internal teams to deliver high-quality and timely benefit-risk activities and outputs.
Qualifications
- Physician’s degree required (MD).
- Experience in pharmacovigilance, safety writing and benefit-risk planning.
- Experience in clinical development and regulatory submissions is an asset.
- Strong project management skills and ability to oversee multiple outputs and deadlines.
- Excellent communication and stakeholder engagement skills, both written and verbal, with the ability to present complex information clearly.
- Demonstrated ability to work collaboratively in cross-functional teams and with external stakeholders.
- Commitment to ethical decision-making and dedication to patient safety.
If you’re ready to make a meaningful impact on patient lives and contribute to patient safety, we invite you to apply and join our team!
About Us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science. Why work with UCB? We don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note if your enquiry does not relate to adjustments; we will not be able to support you through this channel.
Patient Safety Lead in Slough employer: UCB
Contact Detail:
UCB Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Patient Safety Lead in Slough
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working at UCB. A friendly chat can open doors and give you insider info on the role.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of patient safety and drug development. Be ready to discuss how your experience aligns with the role and show your passion for improving patient outcomes.
✨Tip Number 3
Showcase your project management skills! Be prepared to share examples of how you've successfully managed multiple outputs and deadlines in past roles. This will highlight your ability to thrive in a cross-functional team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our team and making a difference in patient safety.
We think you need these skills to ace Patient Safety Lead in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Patient Safety Lead role. Highlight your experience in pharmacovigilance and safety writing, as well as any relevant project management skills.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about patient safety and how your background makes you a great fit for our team. Be sure to mention specific examples of your work in clinical development or regulatory submissions.
Showcase Your Communication Skills: Since excellent communication is key for this role, make sure your application materials are clear and concise. Use straightforward language and structure your documents well to demonstrate your ability to present complex information clearly.
Apply Through Our Website: We encourage you to apply directly through our website. This way, you can ensure your application reaches us quickly and efficiently, and you’ll have access to all the latest updates about the role and our company.
How to prepare for a job interview at UCB
✨Know Your Stuff
Make sure you brush up on your knowledge of pharmacovigilance and benefit-risk assessments. Familiarise yourself with recent developments in patient safety and drug development, as well as any relevant regulations. This will show that you're not just interested in the role but are also proactive about staying informed.
✨Showcase Your Collaboration Skills
Since you'll be working in a cross-functional team, be ready to discuss your experience collaborating with different stakeholders. Prepare examples that highlight your communication skills and how you've successfully worked with others to achieve common goals. This will demonstrate that you can thrive in a team-oriented environment.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving abilities, especially regarding risk management strategies. Think of specific scenarios where you've had to analyse data or make decisions under pressure. Practising these responses will help you articulate your thought process clearly during the interview.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready about the company's approach to patient safety or their current projects. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your values, particularly around patient care and ethical decision-making.
