Medical Safety Lead
Basel (City)
Key information
- Publication date:20 November 2025
- Workload:100%
- Place of work:Basel (City)
Job summary
Join Novartis and make a profound impact on patient safety! This is an extraordinary opportunity in a dynamic work environment.
Tasks
- Spearhead safety evaluations and collaborate with global teams.
- Conduct medical assessments and follow-ups on individual cases.
- Contribute to regulatory responses and prepare safety data.
Skills
- Master's or PhD in a relevant field with 4 years of experience.
- Strong knowledge of clinical trial methodology and regulations.
- Proven ability to interpret and present safety data effectively.
Is this helpful?
Summary
As a Medical Safety Lead, you'll spearhead safety evaluations, collaborate with dynamic global teams, and craft safety strategies that not only protect patients but also drive groundbreaking medical innovation.
Be a part of something extraordinary!
About the Role
Location: Basel, Switzerland or London, The Westworks, UK
Working model: Hybrid
Key Responsibilities:
- Monitor clinical safety data, literature, and case reports to identify potential safety signals
- Conduct medical assessments for individual cases, including follow-ups and quality defect evaluations
- Perform signal detection and evaluation using aggregate and single-case data
- Contribute to regulatory responses and prepare safety data for health authority reviews
- Support safety input for core data sheets and related regulatory documentation
- Provide medical input for aggregate safety reports and risk management plans
- Collaborate with cross-functional teams on clinical safety deliverables and study documentation
- Offer expert evaluation on adverse event reports and guide pharmacovigilance operations
Essential Requirements:
- Master of Science / PharmD / PhD in a relevant field
- Fluent in spoken and written English; additional language skills are a plus
- Minimum 4 years of experience in drug development, including 2 years in patient safety
- Strong knowledge of clinical trial methodology, regulatory requirements, and scientific analysis
- Proven ability to interpret and present safety data clearly and effectively
- Experience contributing to clinical safety assessments and regulatory safety reports
Desirable Skills:
- Medical degree (MBBS or MD) with specialization preferred
- Experience managing clinical safety issues
Accessibility and Inclusion
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 E-Mail schreiben and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Ready to make a difference? Apply now and help us reimagine medicine for millions of patients worldwide.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external)
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
About the company
Basel (City)
Reviews
- Management style1.0
- Salary and benefits3.0
- Career opportunities2.0
- Working atmosphere1.0