Resumes
Resumes

Global Regulatory Therapeutic Area Lead - Immunology And Neurology
View pageLocation:
Collegeville, PA
Industry:
Pharmaceuticals
Work:
Csl Behring
Global Regulatory Therapeutic Area Lead - Immunology and Neurology
Galera Therapeutics, Inc. Apr 2018 - Jul 2019
Vice President, Head of Regulatory Affairs
Venatorx Pharmaceuticals Inc. Apr 2018 - Jul 2019
Vp, Regulatory Affairs
Galera Therapeutics, Inc. Oct 2016 - Apr 2018
Senior Director, Regulatory Affairs
Pfizer Jun 2013 - Sep 2016
Director of Regulatory Affairs, Global Team Lead
Global Regulatory Therapeutic Area Lead - Immunology and Neurology
Galera Therapeutics, Inc. Apr 2018 - Jul 2019
Vice President, Head of Regulatory Affairs
Venatorx Pharmaceuticals Inc. Apr 2018 - Jul 2019
Vp, Regulatory Affairs
Galera Therapeutics, Inc. Oct 2016 - Apr 2018
Senior Director, Regulatory Affairs
Pfizer Jun 2013 - Sep 2016
Director of Regulatory Affairs, Global Team Lead
Education:
The Johns Hopkins University - Carey Business School 2004 - 2007
Master of Business Administration, Masters, Biotechnology Thomas Jefferson University 2003 - 2003
Master of Science, Masters, Chemistry Wake Forest University 1997 - 2000
Bachelors, Bachelor of Science, Biology, Chemistry
Master of Business Administration, Masters, Biotechnology Thomas Jefferson University 2003 - 2003
Master of Science, Masters, Chemistry Wake Forest University 1997 - 2000
Bachelors, Bachelor of Science, Biology, Chemistry
Skills:
Ind
Regulatory Submissions
Clinical Trials
Drug Development
Biotechnology
Regulatory Affairs
Clinical Development
Fda
Biopharmaceuticals
Neuroscience
Pharmaceutical Industry
Gcp
Ectd
Pharmacovigilance
Regulatory Requirements
Life Sciences
Good Clinical Practice
U.s. Food and Drug Administration
Electronic Common Technical Document
Regulatory Submissions
Clinical Trials
Drug Development
Biotechnology
Regulatory Affairs
Clinical Development
Fda
Biopharmaceuticals
Neuroscience
Pharmaceutical Industry
Gcp
Ectd
Pharmacovigilance
Regulatory Requirements
Life Sciences
Good Clinical Practice
U.s. Food and Drug Administration
Electronic Common Technical Document