Eliza Okoria's Location
London, GB
Eliza Okoria's Work
- Lead Regulatory Affairs Consultant @ Roche
- Regulatory Affairs Consultant @ Amgen
- Associate Director Regulatory Affairs @ Alexion Pharmaceuticals, Inc.
- Manager, Regulatory Development @ Norgine
- Regulatory Affairs Manager @ Daiichi Sankyo, Inc.
- Regulatory Affairs Project Manager @ Syneos Health
- Senior Regulatory Affairs Associate @ Syneos Health
- Regulatory Affairs Executive @ PPD
Eliza Okoria's Education
- Kingston University
Master of Science (MSc) (Pharmaceutical Sciences and Management Studies)
2010 - 2011 - University of Westminster
Bsc (Pharmacology)
2002 - 2006
Eliza Okoria's Skills
- Regulatory Submissions
- Regulatory Affairs
- GCP
- Clinical Trials
- eCTD
- Pharmacovigilance
- Regulatory Requirements
- Pharmaceutical Industry
- Clinical Development
- CRO
Eliza Okoria's Summary
Eliza Okoria, based in London, GB, is currently a Lead Regulatory Affairs Consultant at Roche, bringing experience from previous roles at Amgen, Alexion Pharmaceuticals, Inc., Norgine and Daiichi Sankyo. Eliza Okoria holds a 2010 - 2011 Master of Science (MSc) in Pharmaceutical Sciences and Management Studies @ Kingston University. With a robust skill set that includes Regulatory Submissions, Regulatory Affairs, GCP, Clinical Trials, eCTD and more, Eliza Okoria contributes valuable insights to the industry. Eliza Okoria has 2 emails on RocketReach.
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