Emma Y. Email
Manager, Regulatory Affairs @ Zoetis
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Emma Y. Location
- Montreal, QC, CA
Emma Y. Work
- 2025 -now Manager, Regulatory Affairs @
- 2024 -2025 Senior Regulatory Affairs Specialist (Acting Manager-Canada and Australia and UK and Israel and Team Lead-Canada) @
- 2023 -2024 Regulatory Affairs Specialist (Acting Manager-Canada and Australia and Team Lead-Canada) @
- 2021 -2024 Regulatory Affairs Specialist (Acting Team Lead for Canada) @
- 2021 -2022 Regulatory Affairs Specialist (Acting Regulatory and Site Activation Specialist for Canada) @
- 2020 -2021 Ethics and Regulatory Affairs Specialist, Infectious and Immune Diseases @
- 2018 -2019 Regulatory Affairs Associate I, Early Stage Clinical Pharmacology Division @
- 2016 -2018 Clinical Pharmacology Associate (Acting Team Lead and Clinical Research Scientist) @
- 2016 -2016 Research Assistant, Clinical Ophthalmology Unit @
- 2016 -2016 Consultant and Coordinator @
- 2015 -2016 Research Assistant, Pharmacoepidemiology @
- 2010 -2014 Laboratory Technician II, Array Technologies Unit @
- 2007 -2011 Pharmacy Technician @
- 2007 -2010 Laboratory Technician I, Sequencing Platform @
- 2007 -2007 Pharmacy Technician @ Desjardins Pharmacy
Emma Y. Education
- Duke University School of Medicine 2024-2024
- Project Management Institute
Project Management Basics
2020-2023 - Université de Montréal
Master of Science (M.Sc.) (Pharmaceutical Sciences, Drug Development)
2015-2016 - Université de Montréal
Specialized Graduate Diploma/Diplôme d'études supérieures spécialisées (D.E.S.S.) (Drug Development: Regulatory Affairs)
2012-2015 - Kriger Research Group International
Clinical Research Professional Development Certificate (Clinical Research Associate Program + Good Clinical Practice (GCP))
2007-2009 - University of Ottawa
Honors Bachelor of Science (Hons. B.Sc.) (Biopharmaceutical Sciences: Genomics)
2003-2007
Emma Y. Skills
- Leadership
- Laboratory
- Sample Management
- Clinical Trials
- Ich Gcp
- Good Laboratory Practice Glp
- Literature Reviews
- Keyboard Skills
- Clinical Pharmacology
- Genomics
- Microsoft PowerPoint
- Clinical Research
- Regulatory Documentation
- Data Analysis
- Good Clinical Practice Gcp
- Biotechnology
- PCR
- Regulatory Affairs
- DNA
- Life Sciences
- Healthcare
- Bilingual
- Polymerase Chain Reaction Pcr
- Scientific Writing
- Pharmacoepidemiology
- Regulatory Requirements
- Molecular Biology
- Microsoft Office
- Lifesciences
- Microsoft Word
- Laboratory Information Management System Lims
- Microsoft Excel
- Drug Development
- Clinical Development
- Time Management
- Microsoft Outlook
- Customer Service
- u.s. Food and Drug Administration Fda
- Regulatory Submissions
- Pharmacology
- Teamwork
- Project Management
- Standard Operating Procedure Sop
- Quality Control
- Research
- Pharmaceutical Industry
- Biochemistry
- Genetics
- DNA sequencing
- DNA microarray
- Sop
- Pharmacokinetics
- Good Clinical Practice
- Polymerase Chain Reaction
- Good Laboratory Practice
- u.s. Food and Drug Administration
- Laboratory Information Management System
Emma Y. Summary
- Emma Y., based in Montreal, QC, CA, is currently a Manager, Regulatory Affairs at Zoetis. Emma Y. brings experience from previous roles at Worldwide Clinical Trials. Emma Y. holds a 2024 - 2024 Duke University School of Medicine. With a robust skill set that includes Leadership, Laboratory, Sample Management, Clinical Trials, Ich Gcp and more. Emma Y. has 3 emails on RocketReach.
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