Krisztina Nemenyi's Location
Boston, Massachusetts, United States
Krisztina Nemenyi's Work
- SVP Regulatory Affairs and Quality @ Cyteir Therapeutics
- Senior Vice President Regulatory Affairs and Quality @ Cyteir Therapeutics
- Vice President, Global Program Lead Oncology @ Takeda Pharmaceuticals
- Vice President, Global Regulatory Affaris, Oncology at Takeda Pharmaceuticals @ Takeda Pharmaceuticals
- Vice President, Regulatory Affairs, Emerging Markets and Marketed Products @ Takeda Pharmaceuticals
- Group Director, Asia Pacific Region, Global Regulatory Affairs, International @ Bristol Myers Squibb
- Director Global Regulatory Affairs, Therapeutic Area Oncology @ Bristol Myers Squibb
- Deputy Director, Global Regulatory Affairs @ Bayer
- Manager and Senior Manager, Global Regulatory Affairs @ Baxter International Inc.
- Senior Regulatory Scientist @ Bayer
Krisztina Nemenyi's Education
- Massachusetts Institute of Technology
Master of Business Administration
2019 - 2021 - University of Vienna
Doctor of Philosophy (Chemical Engineering, Chemistry)
1998 - Budapest University of Technology and Economics
Master of Science (Chemical Engineering, Biochemistry)
1994
Krisztina Nemenyi's Skills
- Regulatory Submissions
- Regulatory Affairs
- Clinical Trials
- Pharmaceutical Industry
- FDA
- Drug Development
- Oncology
- Clinical Development
- Biotechnology
- Strategy
Krisztina Nemenyi's Summary
Krisztina Nemenyi, based in Boston, Massachusetts, United States, is currently a SVP Regulatory Affairs and Quality at Cyteir Therapeutics, bringing experience from previous roles at Cyteir Therapeutics and Takeda Pharmaceuticals. Krisztina Nemenyi holds a 2019 - 2021 Master of Business Administration @ Massachusetts Institute of Technology. With a robust skill set that includes Regulatory Submissions, Regulatory Affairs, Clinical Trials, Pharmaceutical Industry, FDA and more, Krisztina Nemenyi contributes valuable insights to the industry. Krisztina Nemenyi has 1 email and 1 mobile phone number on RocketReach.
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