Associate Director, Safety Science
Infos sur l'emploi
- Date de publication :29 juillet 2025
- Taux d'activité :100%
- Lieu de travail :Basel (City)
Résumé de l'emploi
Responsable du programme de surveillance des médicaments à Novartis. Rejoignez un environnement hybride à Bâle, Suisse.
Tâches
- Diriger des projets scientifiques sur la sécurité des médicaments.
- Intégrer des connaissances sur la sécurité dans les activités de développement.
- Collaborer avec des experts pour améliorer les normes de sécurité.
Compétences
- Diplôme médical ou doctorat avec expérience en sécurité des médicaments.
- Compétences en leadership dans des équipes multiculturelles.
- Compréhension des méthodologies d'essai clinique et normes réglementaires.
Est-ce utile ?
Summary
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
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 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.
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
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