Thomas Wimmer Location
- Zürich, ZH, CH
Thomas Wimmer Work
- 2023 -now Data Management Lead, Director @
- 2020 -2023 Head of Regulatory Affairs Infrastructure @
- 2017 -2020 Senior Manager, Regulatory Information Management (RIM) Lead, Global Regulatory Operations @
- 2017 -2020 Senior Manager Global Regulatory Operations @
- 2015 -2017 Manager Regulatory Operations @
- 2013 -2015 Regulatory Affairs Specialist and Operations @
- 2010 -2013 Regulatory Submissions Assistant @
- 2007 -2010 Regulatory Affairs Assistant @ Grünenthal
- 2000 -2007 Chemical Technician @ Grünenthal
Thomas Wimmer Education
- Regulatory Affairs Professional Society (RAPS)
Regulatory Affairs Certificate: Pharmaceuticals
2013-2013 - Industrie- und Handelskammer Cologne
Train-the-Trainer
2006-2006 - Berufskolleg Stolberg/Simmerath
Chemical Technician
2000-2003
Thomas Wimmer Skills
- Regulatory Submissions
- MAA
- eCTD
- Regulatory Affairs
- NDA
- FDA
- Quality Control
- Regulatory Requirements
- Pharmacovigilance
- GCP
- Drug Development
- Pharmaceutical Industry
- IND
- Sop
- GMP
- Lifesciences
- NeeS
- Electronic Data Management
- FDA ESG Web Trader
- EMA Web Client
- Centralized Procedure
- MRP
- Pharmaindustrie
- Arzneimittelzulassung
- Marktzulassung
- Gute klinische Praxis
- Life Sciences
- Arzneimittelentwicklung
- Rechtliche Anforderungen
- Development
- PowerPoint
- Public Speaking
- Operations
- Microsoft Excel
- Electronic Data
- Project Management
- Research
- Regulatory Information Management
Thomas Wimmer Summary
- Thomas Wimmer, based in Zürich, ZH, CH, is currently a Data Management Lead, Director at CSL. Thomas Wimmer brings experience from previous roles at Vifor Pharma and Alexion Pharmaceuticals, Inc.. Thomas Wimmer holds a 2013 - 2013 Regulatory Affairs Certificate: Pharmaceuticals @ Regulatory Affairs Professional Society (RAPS). With a robust skill set that includes Regulatory Submissions, MAA, eCTD, Regulatory Affairs, NDA and more. Thomas Wimmer has 3 emails on RocketReach.
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