Sibylle Jennings's Location
Basel, BS, CH
Sibylle Jennings's Work
- Global Therapeutic Area Lead, Radioligand Therapy @ Novartis Oncology
- Global Head Regulatory Affairs, Advanced Accelerator Applications, a Novartis Company @ Advanced Accelerator Applications
- Global Therapeutic Area Lead GI and GU and Melanoma @ Novartis Oncology
- Senior Global Program Regulatory Director, Afinitor and Votrient and PDR001 @ Novartis Oncology
- Senior Early Development Regulatory Director @ Novartis
- Senior Global Program Regulatory Director @ Novartis Oncology
- Global Program Regulatory Director @ Novartis Oncology
- Senior Associate Director, Regulatory Affairs @ Novartis Oncology
- Associate Director, Regulatory Affairs @ Berlex (formerly US CPO of Schering AG, now US CPO of Bayer Healthcare)
- Regulatory Affairs Manager @ Bayer HealthCare (formerly Schering AG)
Sibylle Jennings's Education
- Heinrich-Heine-Universität Düsseldorf
Doctor of Philosophy (Ph.D.) (Anti-inflammatory Chinese Medicinal Plants)
1993 - 1998 - Ludwig-Maximilians Universität München
Staatsexamen (Pharmacy)
1986 - 1991 - Edith-Stein-Gymnasium
High School
1977 - 1986
Sibylle Jennings's Skills
- Oncology
- Clinical Trials
- Pharmacovigilance
- Regulatory Submissions
- Pharmaceutical Industry
- Regulatory Affairs
- Drug Development
- Clinical Development
- Early Development
Sibylle Jennings's Summary
Sibylle Jennings, based in Basel, BS, CH, is currently a Global Therapeutic Area Lead, Radioligand Therapy at Novartis Oncology, bringing experience from previous roles at Advanced Accelerator Applications, Novartis Oncology and Novartis. Sibylle Jennings holds a 1993 - 1998 Doctor of Philosophy (Ph.D.) in Anti-inflammatory Chinese Medicinal Plants @ Heinrich-Heine-Universität Düsseldorf. With a robust skill set that includes Oncology, Clinical Trials, Pharmacovigilance, Regulatory Submissions, Pharmaceutical Industry and more, Sibylle Jennings contributes valuable insights to the industry. Sibylle Jennings has 2 emails on RocketReach.
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