Urte Gayko's Location
San Carlos, CA, US
Urte Gayko's Work
- Chief of Regulatory, Quality and PV @ Summit Therapeutics, Inc.
- Head of Regulatory, Quality and Safety @ Summit Therapeutics, Inc.
- Board Member @ Summit Therapeutics, Inc.
- Sr VP, Drug Development and Regulatory Affairs @ Nektar Therapeutics
- Global Head of Regulatory Affairs and Pharmacovigilance @ Pharmacyclics, an AbbVie Company
- Sr. VP Global Regulatory Affairs @ Pharmacyclics, an AbbVie Company
- VP Global Regulatory Affairs @ Pharmacyclics, an AbbVie Company
- VP Regulatory and Clinical Affairs @ Nodality Inc.
- Director Regulatory Affairs @ Amgen
- Clinical Scientist and Associate Director, Global Program Manager @ Amgen
Urte Gayko's Education
- Harvard University
PhD (Molecular and Cellular Biology)
Urte Gayko's Skills
- Regulatory Affairs
- Oncology
- Drug Development
- Clinical Development
- Biotechnology
- IND
- Regulatory Submissions
- Pharmaceutical Industry
- Lifesciences
- Biopharmaceuticals
Urte Gayko's Summary
Urte Gayko, based in San Carlos, CA, US, is currently a Chief of Regulatory, Quality and PV at Summit Therapeutics, Inc., bringing experience from previous roles at Summit Therapeutics, Nektar Therapeutics and Pharmacyclics LLC an Abbvie Company. Urte Gayko holds a PhD in Molecular and Cellular Biology @ Harvard University. With a robust skill set that includes Regulatory Affairs, Oncology, Drug Development, Clinical Development, Biotechnology and more, Urte Gayko contributes valuable insights to the industry. Urte Gayko has 6 emails and 1 mobile phone number on RocketReach.
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