Theresa Tran

Associate Director Regulatory Affairs

Theresa Tran is a skilled expert, working in Alnylam Pharmaceuticals main office of which is in 518. as a Associate Director Regulatory Affairs since 2019. This expert has earned professional experience in more than nine positions at various companies. Theresa Tran went to the University of the Sciences in Philadelphia and got education there from 2008. Seattle, Washington is the city, where this person was known to be living. This expert's email address and phone number are accessed through this website on demand.
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Teresa Tran

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Contact Information

Last Update
Jul 3, 2022
Email
th**@gmail.com, th**@gilead.com
Location
Seattle, WA

Workplace

Alnylam Pharmaceuticals
Associate Director Regulatory Affairs

Cambridge, MA

Industry

Biotechnology, Biopharmaceutical Research, Commercial Physical Research, Biotechnical Research & Pharmaceutical Preparations, Mfg of Pharmaceutical Preparations and Biotechnical Research, Mfg Pharmaceutical Preparations and Biotechnical Research, Pharmaceutical Preparation Mfg

Work History

Associate Director Regulatory Affairs

675 west Kendall St, Cambridge, MA 02142
from Jan 2019

Associate Director, Regulatory Affairs

101 Carnegie Ctr SUITE 101, Princeton, NJ 08540
Aug 2017 — Jan 2019

Senior Manager, Regulatory Affairs

1180 Veterans Blvd, South San Francisco, CA 94080
Mar 2016 — May 2017

Associate Manager, Regulatory Affairs at Gilead Sciences

333 Lakeside Dr, Foster City, CA 94404
Sep 2014 — Mar 2016

Regulatory Affairs Manager

New Jersey
Jul 2012 — Aug 2014

Regulatory Affairs Team Leader

Sep 2009 — Jul 2012

Regulatory Affairs Specialist

Yardley, PA
May 2008 — Sep 2009

Staff Pharmacist

2000 — Aug 2010

Regulatory Affairs Associate III

2000 — Sep 2009

Education

Doctor of Pharmacy

Philadelphia, PA
from May 2008

Occupations

Executive
Deputy Director
Scientist
Biotechnology Professional
Deputy Manager
Chief Executive
Biologist
Biological Scientist

Skills

Regulatory Affairs
Regulatory Submissions
Pharmaceutical Industry
Pharmaceutics
Ectd
Fda
Regulatory Requirements
Sop
Gmp
Anda
Clinical Trials
Clinical Development
Pharmacovigilance
Gcp
U.s. Food and Drug Administration
Standard Operating Procedure
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