Resumes
Resumes

Vice President And Head Of Regulatory Affairs
View pageLocation:
10 Winding Way, Chester, NJ 07930
Industry:
Pharmaceuticals
Work:
Applied Therapeutics
Vice President and Head of Regulatory Affairs
Eagle Pharmaceuticals, Inc. 2009 - 2011
Vice President, Regulatory and Clinical Affairs
Ferring Pharmaceuticals 2009 - 2011
Vice President, Regulatory Affairs Us
Sapphire Therapeutics, Inc. 2007 - 2009
Vice President, Regulatory Affairs
Berlex Laboratories 1994 - 2003
Director, Regulatory Affairs
Vice President and Head of Regulatory Affairs
Eagle Pharmaceuticals, Inc. 2009 - 2011
Vice President, Regulatory and Clinical Affairs
Ferring Pharmaceuticals 2009 - 2011
Vice President, Regulatory Affairs Us
Sapphire Therapeutics, Inc. 2007 - 2009
Vice President, Regulatory Affairs
Berlex Laboratories 1994 - 2003
Director, Regulatory Affairs
Education:
University of Maryland - Baltimore 1994 - 1998
Doctorates, Doctor of Pharmacy, Pharmacy The Wharton School 1990 - 1992
Master of Business Administration, Masters, Business Rutgers University 1977 - 1982
Master of Science, Masters, Bachelors, Bachelor of Science, Pharmacy
Doctorates, Doctor of Pharmacy, Pharmacy The Wharton School 1990 - 1992
Master of Business Administration, Masters, Business Rutgers University 1977 - 1982
Master of Science, Masters, Bachelors, Bachelor of Science, Pharmacy
Skills:
Regulatory Affairs
Pharmaceutical Industry
Drug Development
Regulatory Submissions
Clinical Development
Fda
Clinical Trials
Biopharmaceuticals
Gmp
Biotechnology
Oncology
Pharmacovigilance
Technology Transfer
Ind
Medical Devices
Cro
Pharmaceutics
Gcp
Lifesciences
Commercialization
21 Cfr Part 11
Infectious Diseases
Clinical Research
Validation
Therapeutic Areas
Medical Affairs
Drug Discovery
Ectd
Sop
Regulatory Requirements
Medical Writing
Change Control
Nda
Ctms
R&D
Capa
Anda
Biologics
Glp
Vaccines
Pharmacology
Immunology
V&V
Dermatology
Cmc Regulatory Affairs
Neurology
Edc
Cmc
Formulation
Pharmaceutical Industry
Drug Development
Regulatory Submissions
Clinical Development
Fda
Clinical Trials
Biopharmaceuticals
Gmp
Biotechnology
Oncology
Pharmacovigilance
Technology Transfer
Ind
Medical Devices
Cro
Pharmaceutics
Gcp
Lifesciences
Commercialization
21 Cfr Part 11
Infectious Diseases
Clinical Research
Validation
Therapeutic Areas
Medical Affairs
Drug Discovery
Ectd
Sop
Regulatory Requirements
Medical Writing
Change Control
Nda
Ctms
R&D
Capa
Anda
Biologics
Glp
Vaccines
Pharmacology
Immunology
V&V
Dermatology
Cmc Regulatory Affairs
Neurology
Edc
Cmc
Formulation
Languages:
English