Description
Job ID
REQ-10056728
Aug 27, 2025
Switzerland
### Summary ###
Verantwortlich für das Arzneimittelüberwachungsprogramm einschließlich der notwendigen Nachverfolgung, Risikobewertung und Produktverwandtwerden zu Berichten über Nebenwirkungen, Aufsicht über die Sicherheit in klinischen Studien und Post-Marketing-Programmen. Beteiligt sich an der Lösung jeglicher rechtlicher Haftung und der Einhaltung behördlicher Vorschriften. Bietet und trägt zur Trend- und Sicherheitssignalerkennung und Risikomanagementbewertung für den Lebenszyklus der Produkte bei. Bietet Sicherheitsunterstützung für die klinischen Entwicklungsteams.
### About the Role ###
**\#LI-Hybrid**
**Location:** Basel, Switzerland
**Working Model:** Hybrid
**Relocation Support:** This role is based in Basel, Switzerland. Novartis is unable to offer relocation support: please only apply if accessible.
## Key Responsibilities ##
* Lead scientific projects and evaluations of safety topics across early development, full development, and marketed products
* Guide mechanistic investigations and integrate safety insights into cross-functional development activities
* Co-lead Safety Science platform meetings such as the Early Safety Hub (ESH) and Early Portfolio Safety Group (EPSG)
* Support preparation and scientific quality of safety board meetings, including Integrated Safety Assessment Board (ISAB) and Medical Safety Review Board (MSRB)
* Review and advise on mechanistic studies, Risk Management Plans, and safety signal action plans
* Contribute to safety training and knowledge sharing within Patient Safety as well as important clinical partner functions (Clinical Development, Translational Medicine and Translational Clinical Oncology)
* Collaborate with internal and external experts to advance safety science standards and practices
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## Essential Requirements ##
* Medical degree (preferred) or PhD with relevant drug safety experience in a pharmaceutical or biotech company
* Peer-reviewed publications in pharmacology, clinical research or safety
* 3-5 years of postdoctoral or clinical experience
* 3-5 years of drug development experience in academia or the pharmaceutical industry
* Proven experience preparing clinical safety assessments and regulatory safety submissions
* Strong leadership in cross-functional, multicultural team environments
* Deep understanding of clinical trial methodology, regulatory standards, and scientific writing
* Fluent in English, both spoken and written
## ##
## Desirable Skills ##
* Understanding of an additional major language (e.g. French or German)
* Experience contributing to external scientific collaborations in drug safety
Ready to shape the future of safety? Apply now and bring your scientific leadership to a team that-s transforming lives.
## 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 inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
**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
Division
Development
Business Unit
Innovative Medicines
Location
Switzerland
Site
Basel (City)
Company / Legal Entity
C028 (FCRS = CH028) Novartis Pharma AG
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regulär
Shift Work
No