Sabrina Girty is a eficient expert, that works in Merck main office of which is in 60. on the position of Director, Global Regulatory Affairs from 2019. Sabrina Girty has earned professional experience in more than seven positions at different companies. Sabrina Girty went to the Northern Kentucky University—Salmon P. Chase College of Law and was studying from 2000 to 2005. Wayne, Pennsylvania is the city, where this expert was known to be located. The person's e-mail and phone can be accessed through this website on demand.
Name variants:
Brina Girty,
Sabby Girty
Last updated Jun 13, 2024
Contact Information
Last Update
Jul 7, 2022
Email
sg**@xanodyne.com, gi**@lycera.com, sg**@shire.com
Location
Wayne, PA
Company
Workplace
Colleagues
Work History
Director, Global Regulatory Affairs
2000 Galloping Hill Rd, Kenilworth, NJ 07033
from Jan 2019
Vice President, Regulatory Affairs
1350 Highland Dr, Ann Arbor, MI 48108
Head of Regulatory Affairs for private biopharmaceutical company. Responsible for developing regulatory strategies for Lycera’s immuno-oncology and autoimmune development programs in alignme...
Sep 2015 — Jan 2019
Senior Director, Regulatory Affairs
Global Regulatory Lead for development programs in the GI, hepatic, and neuroscience (rare disease) therapeutic areas. Responsible for developing and directing the global regulatory strategy...
Aug 1, 2014 — Sep 2015
Director, Regulatory Affairs
Responsible for developing and directing objectives, policies, and programs pertaining to development and marketing of drug products in the US and globally.
Apr 2012 — Aug 2014
Director, Regulatory Affairs
1 Riverfront Plz, Newport, KY
Associate Director: April 2007
December 2009
Director: January 2010
March 2011
Executive Director: April 2011
April 2012
Apr 2007 — Apr 2012
Director, Regulatory Affairs and Quality Assurance
5375 Medpace Way, Cincinnati, OH 45201
Jan 1999 — Apr 2007
Senior Quality Assurance Scientist
5375 Medpace Way, Cincinnati, OH 45201
QA Scientist: August 1996
January 1998 Senior QA Scientist: January 1998
January 1999
Aug 1996 — Jan 1999
Education
1992 — 1996
Occupations
Executive
Director
Vice President
Operations Manager
Chief Executive
Skills
Regulatory Affairs
Clinical Trials
Regulatory Submissions
Pharmaceutical Industry
Fda
Drug Development
Cross Functional Team Leadership
Due Diligence
Regulatory Requirements
Clinical Development
Biotechnology
Gcp
Quality Assurance
Strategy
Regulations
Risk Management
Oncology
Sop
Auditing
Medical Devices
Technology Transfer