Clinical Development and Quality/Compliance Professional
Greater Boston Area
Sage Therapeutics
Director, GCP GLP Research Quality Assurance
August 2017 to March 2018
Cambridge, US
NJ Department of Education, Refugee Assistance Program
Bilingual Counselor/ESL Teacher
1984 to 1986
Plainfield, NJ
Alnylam Pharmaceuticals
Associate Director, Clinical Quality Assurance
April 2015 to October 2015
Cambridge, MA
Genzyme
Data Program Manager
1996 to 1997
Cambridge, MA
Massachusetts General Hospital
Research Technician
1986 to 1989
Boston, MA
LFB USA
Sr. Director, Head of GxP Compliance
February 2017 to August 2017
Framingham, Massachusetts
LFB USA
Director, Global Head Clinical QA
December 2015 to January 2017
Framingham, Massachusetts
Vertex Pharmaceuticals
Principal Data Manager
1999 to 2004
Cambridge, MA
Merck
Clinical Data Manager
1994 to 1996
Rahway, NJ
Merck
Staff Immunologist
1989 to 1995
Rahway, NJ
Kummer Consulting LLC
Senior Consultant, New R&D Models
January 2013 to December 2015
Belmont, MA
Biogen
Senior Manager, R&D Compliance Quality Standards
January 2012 to October 2014
Cambridge, MA
Biogen
Clinical Data Program Manager
August 2004 to January 2012
Cambridge, MA
Pfizer
Clinical Data Associate
1996 to 1999
Cambridge, MA
What company does Mai Nguyen work for?
Mai Nguyen works for Sage Therapeutics
What is Mai Nguyen's role at Sage Therapeutics?
Mai Nguyen is Director, GCP GLP Research Quality Assurance
What industry does Mai Nguyen work in?
Mai Nguyen works in the Pharmaceuticals industry.
Who are Mai Nguyen's colleagues?
Mai Nguyen's colleagues are Fernanda Giupponi, Melanie Fronk, Michael Megna, Paige Graves, Pat Nagle, Jose Toscano, Debra SPHR, Kerry Biron, and Jillian P.
📖 Summary
Director, GCP GLP Research Quality Assurance @ Sage Therapeutics From August 2017 to March 2018 (8 months) Cambridge, USBilingual Counselor/ESL Teacher @ NJ Department of Education, Refugee Assistance Program Provided social services and English as a Second Language training to refugees/immigrants from SE Asia, Cuba and Afghanistan From 1984 to 1986 (2 years) Plainfield, NJAssociate Director, Clinical Quality Assurance @ Alnylam Pharmaceuticals From April 2015 to October 2015 (7 months) Cambridge, MAData Program Manager @ Genzyme Managed patient registry for Ceredase™ and Cerazyme™ (Gaucher disease) From 1996 to 1997 (1 year) Cambridge, MAResearch Technician @ Massachusetts General Hospital Studied cytoskeletal proteins involvement in human cancer metastases and AIDS From 1986 to 1989 (3 years) Boston, MASr. Director, Head of GxP Compliance @ LFB USA From February 2017 to August 2017 (7 months) Framingham, MassachusettsDirector, Global Head Clinical QA @ LFB USA From December 2015 to January 2017 (1 year 2 months) Framingham, MassachusettsPrincipal Data Manager @ Vertex Pharmaceuticals Lead strategic builds during company’s critical growth phase, e.g. CRO partnerships, key technology implementation (e.g. remote data capture, medical coding, metrics, data integrity). From 1999 to 2004 (5 years) Cambridge, MAClinical Data Manager @ Merck Managed studies that supported the approvals of Propecia™ (male pattern baldness) and Fosamax™ (osteoporosis). From 1994 to 1996 (2 years) Rahway, NJStaff Immunologist @ Merck Studied immunological signals in cells to develop therapy for transplant rejection and autoimmunity diseases. From 1989 to 1995 (6 years) Rahway, NJSenior Consultant, New R&D Models @ Kummer Consulting LLC Develop knowledge sharing models for the biotech industry to deliver innovation. From January 2013 to December 2015 (3 years) Belmont, MASenior Manager, R&D Compliance Quality Standards @ Biogen Inspection readiness, quality risk management/compliance to FDA, MHRA, PMDA, CFDA regulations From January 2012 to October 2014 (2 years 10 months) Cambridge, MAClinical Data Program Manager @ Biogen Optimize business processes to support fast-competing clinical trials. Lead development of therapeutic area data standards to streamline end to end data collection and reporting. Lead teams in challenging projects that delivered high value outcomes. From August 2004 to January 2012 (7 years 6 months) Cambridge, MAClinical Data Associate @ Pfizer Managed late stage trials that supported the approval of Neumega™ From 1996 to 1999 (3 years) Cambridge, MA
Extraversion (E), Intuition (N), Thinking (T), Judging (J)
2 year(s), 8 month(s)
Unlikely
Likely
There's 73% chance that Mai Nguyen is seeking for new opportunities
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