Experience

Vir Biotechnology, Inc.

• United States
• Biotechnology Research
• 300 - 400 Employee

• Manager, Regulatory Affairs

  • Oct 2020 - Present

  San Francisco, California, United States



AbbVie

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Senior Analyst, Global Regulatory Strategy

  • May 2020 - Sep 2020

  Irvine, California, United States



Allergan

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Senior Analyst, Global Regulatory Affairs

  • Apr 2019 - May 2020

  Irvine, California, United States

• Postdoctoral Fellow in Global Regulatory Affairs

  • Jul 2018 - Jun 2019

  Irvine, California, United States The one-year Global Regulatory Affairs (GRA) Fellowship provides hands-on experience constructing global regulatory submission documents from the initial stages of document preparation to final submission. The fellow is a key member of the core team and shares responsibility for facilitating timely submission and publishing of documents to regulatory agencies around the globe. In addition, the fellow will have opportunities to manage several projects inside and outside of GRA as part of a… Show more The one-year Global Regulatory Affairs (GRA) Fellowship provides hands-on experience constructing global regulatory submission documents from the initial stages of document preparation to final submission. The fellow is a key member of the core team and shares responsibility for facilitating timely submission and publishing of documents to regulatory agencies around the globe. In addition, the fellow will have opportunities to manage several projects inside and outside of GRA as part of a comprehensive training program. -Assemble and manage regulatory documents in electronic Common Technical Documents (eCTD) format that meet regulatory standards -Interact with Global Regulatory Affairs, Clinical Development, Project Management, Clinical Manufacturing, Method Development, Process Development, Analytical Testing, Research and Development, Drug Safety, Toxicology, Clinical Pharmacokinetics, Labeling, Quality Assurance, Publishing and Marketing to discuss issues specific to Pharmaceutical Sciences, and apply the information acquired -Review and discuss analytical method development, validation and implementation with chemistry, manufacturing and controls team leaders and analytical scientists



Kaiser Permanente

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Intern Pharmacist

  • Dec 2014 - Jun 2018

  Los Angeles, California, United States Under direct supervision of a licensed pharmacist dispenses, compounds, procures, stores & distributes pharmacy products. Consults w/ patients & medical personnel regarding medication therapy. Provides pharmaceutical care for hospitalized or ambulatory patients as assigned. Provides medical personnel & patients w/ medication information & product identification.



FDA

• United States
• Government Administration
• 700 & Above Employee

• Pharmacy Student Intern

  • Feb 2018 - Mar 2018

  Silver Spring, Maryland, United States



Avanir Pharmaceuticals

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Medical Affairs Intern

  • Jun 2017 - Aug 2017

  Aliso Viejo, California, United States