Lynne Fahey Mcgrath

Strategic Partner

Since 2018, Lynne Fahey Mcgrath has been working in Foxkiser. This expert is an experienced Strategic Partner with over 36 years of work experience. According to Lynne's resume and work profile, Lynne Fahey Mcgrath has worked at more than 11 companies with numerous backgrounds and gained various skills. Lynne attended school at the Rutgers Robert Wood Johnson Medical School from 1994 to 1994. Lynne can be found in Washington, DC – where the professional is currently located. You can search for the person's email address and number. We can also provide you exhaustive contact information upon request.
Name variants:
Lynn Mcgrath, Caroline Mcgrath, Linda Mcgrath
Last updated Jun 05, 2024

Contact Information

Last Update
Jul 5, 2022
Email
ly**@novartis.com, lm**@regenxbio.com
Location
Washington, DC
Company

Workplace

Strategic Partner

Industry

Biotechnology

Work History

Strategic Partner

from Oct 2018

Vice President, Regulatory Affairs

Maryland
Lead regulatory strategy for biotechnology company specializing in gene therapy
May 2015 — Jul 2018

Global Head Regulatory Affairs, Novartis Consumer Health

Dec 1, 2012 — Apr 2015

Na Head, Vice-President, Regulatory Affairs - Oncology

Jul 2008 — Dec 2012

Executive Director, Global Drug Regulatory Affairs, Oncology

2003 — 2008

Global Regulatory Affairs, Oncology

New York, NY
2002 — 2003

Associate Director

2001 — 2002

Manager International Regulatory Affairs

1999 — 2001

Assistant Professor, Department of Community Medicine

Public Health Risk Assessment research
1996 — 1999

Manager Health Risk Assessment

Government Affairs, Health Policy, Safety Assessment, Health and Environmental Risk Assessment
1989 — 1996

Safety Scientist

2000 Galloping Hill Rd, Kenilworth, NJ 07033
Manage pre-clinical activities for support of registration of INDS and new products
Jan 1981 — Dec 1988

Occupations

Executive
Partner
Scientist
Biotechnology Professional
Vice President
Chief Executive
Biologist
Biological Scientist

Skills

Regulatory Affairs
Pharmaceutical Industry
Oncology
Regulatory Submissions
Clinical Trials
Drug Development
Clinical Development
Regulatory Requirements
Ind
Fda
Gcp
Policy
Risk Assessment
Nda
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