At a Glance
- Tasks: Lead safety strategies and collaborate with global teams to enhance patient safety.
- Company: Join Novartis, a forward-thinking pharmaceutical leader committed to innovation.
- Benefits: Enjoy hybrid work, competitive salary, and opportunities for personal and professional growth.
- Other info: Dynamic role with excellent career advancement opportunities in a multicultural environment.
- Why this job: Make a real impact in patient safety while working with cutting-edge technology.
- Qualifications: Medical degree preferred; experience in drug development and safety management required.
The predicted salary is between 80000 - 100000 € per year.
Novartis is seeking passionate individuals to join our innovative team. You will work with cutting‑edge technology, collaborate with experts, and drive excellence in patient safety. If you’re eager to advance your career and be part of a forward‑thinking company, we want you on our team.
About The Role
This is a director level role and can be based in Basel, Switzerland, London, UK, or Barcelona, Spain. Location: Basel, Switzerland. Working pattern: Hybrid.
Key Responsibilities
- Safety Input and Team Participation: Provide expert safety input to the clinical development program for assigned projects/products and actively participate in the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Lead the Safety Management Team (SMT). Responsible for managing safety issues from the formation of the GPT through Life Cycle Management.
- Safety Strategy Preparation: Own the projects/products safety strategy and lead the production of medical safety deliverables.
- Core Global Labelling: Responsible for initial development and ongoing maintenance of safety information in Core Data Sheet, addressing safety issues in all project/product indications.
- Signal Detection and Safety Management: Oversee overall signal detection, monitoring, evaluation, interpretation, and appropriate management of safety information, based on data from all relevant sources.
- Regulatory and Professional Inquiries: Lead the preparation of the safety strategy for health authority responses and collaborate with other project team members. Respond to inquiries from regulatory authorities or healthcare professionals regarding safety issues.
- Departmental and Functional Goals: Contribute to and often lead the development of departmental and functional/business unit goals and objectives. Proactively engage in the development of competencies across the Medical Safety Function.
Role Requirements
- Medical Degree or equivalent is preferred; PhD, PharmD or equivalent graduate level health care professional degree required.
- 3 years clinical experience postdoctoral.
- At least 5 years’ experience in drug development within a major pharmaceutical company, including:
- A minimum of 2 years in a global role, and
- At least 2 years’ experience in drug safety in an operational or medical capacity.
- Experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics, and writing of publications.
- Expertise in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information.
- Experience with safety or other issue management.
- Experience in leading cross‑functional, multicultural teams.
Languages
- Fluent English (both spoken and written) is mandatory.
Additional Desirable Skills
- Additional languages are desirable.
- Oncology experience would be an advantage.
Accessibility And Accommodation
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e‑mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Benefits and Rewards
Learn about all the ways we’ll help you thrive personally and professionally.
Global Program Safety Lead - RLT in London employer: Novartis UK
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic work environment in Basel, Switzerland, where innovation meets collaboration. Our hybrid working model promotes flexibility, while our commitment to employee growth ensures that you will have access to continuous learning and development opportunities. Join us to be part of a forward-thinking team dedicated to advancing patient safety and making a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Global Program Safety Lead - RLT in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the industry on LinkedIn or at events. A friendly chat can open doors that applications alone can't.
✨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Know your stuff about Novartis and be ready to discuss how your experience aligns with their goals.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online platforms. The more comfortable you are, the better you'll perform when it counts.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining the team.
We think you need these skills to ace Global Program Safety Lead - RLT in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the job description. Highlight your clinical experience and any relevant safety management roles you've held. We want to see how you can contribute to our innovative team!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about patient safety and how your background aligns with our goals. Keep it engaging and personal – we love to see your enthusiasm!
Showcase Your Teamwork Skills:Since this role involves leading cross-functional teams, make sure to highlight your collaborative experiences. Share examples of how you've worked with diverse groups to achieve common goals. We value teamwork at StudySmarter!
Apply Through Our Website:Don't forget to apply through our official website! It’s the best way for us to receive your application and ensure it gets the attention it deserves. We can't wait to see what you bring to the table!
How to prepare for a job interview at Novartis UK
✨Know Your Stuff
Make sure you brush up on your knowledge of drug development and safety management. Familiarise yourself with the latest trends in clinical trial methodology and regulatory requirements, as these will likely come up during the interview.
✨Showcase Your Experience
Be ready to discuss your past experiences in leading cross-functional teams and managing safety issues. Prepare specific examples that highlight your contributions and how they align with the responsibilities of the Global Program Safety Lead role.
✨Ask Insightful Questions
Prepare thoughtful questions about Novartis' approach to patient safety and their current projects. This shows your genuine interest in the company and helps you gauge if it’s the right fit for you.
✨Practice Your Communication Skills
Since fluency in English is mandatory, practice articulating your thoughts clearly and confidently. You might also want to prepare for potential questions about your experience in oncology or any additional languages you speak.
