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Marc Wiles Location
United States
Marc Wiles Work
Global Head of Regulatory Affairs @ (August 2024 - Present)
Sr. VP, Regulatory Affairs @ (December 2022 - August 2024)
Vice President Regulatory Affairs @ (February 2021 - December 2022)
Senior Director, Global Regulatory Lead - Pharmaceuticals @ (November 2018 - February 2021)
Vice President, Scientific and Regulatory Affairs @ Camargo Pharmaceutical Services (May 2015 - October 2018)
General Manager @ (February 2014 - March 2015)
Director and General Manager @ ERA Consulting (UK) Ltd. (February 2012 - February 2014)
Sr. Vice President, Operations @ (January 2011 - February 2012)
Head of Toxicology @ (April 2009 - September 2010)
Sr. Director, Nonclinical Development @ Shire HGT (September 2007 - September 2008)
Sr. Director Preclinica and Nonclinical R and D @ (December 2004 - September 2007)
Sr. Cell Biologist and Molecular Pharmacologist to Director Cell Biology and Principle Investigator @ NeXstar / Gilead / OSI Pharmaceuticals (August 1995 - November 2004)
Post-Doc @ Parke-Davis (January 1991 - January 1993)
Marc Wiles Education
Boston University
PhD (Cell Biology, Microvascular Physiology)
1986-1991
Macalester College
BA (Biology, Chemistry - Highest Honors)
1982-1986
Marc Wiles Skills
Assay Development
Biochemistry
Biologics
Biopharmaceuticals
Biotechnology
CRO
CRO Management
Cancer Research
Cell
Cell Biology
Cell Culture
Clinical Development
Drug Delivery
Drug Development
Drug Discovery
Drug Metabolism
ELISA
EU Regulatory
Ex-US Regulatory (UK/CAN/N.A./S.A./APAC/ECEMEA)
FDA
GLP
GMP
Global Regulatory Affairs Expertise and Hands On Experience
Global Regulatory Compliance
Good Laboratory Practice (GLP)
IND
Immunoassays
Immunology
In Vitro
In Vivo
Life Sciences
Lifesciences
Molecular Biology
Oncology
Pharmaceutical Industry
Pharmacokinetics
Pharmacology
Pharmacovigilance
Product Development
Protein Chemistry
R&D
Regulatory Affairs
Regulatory Submissions
Research and Development (R&D)
Technology Transfer
Toxicology
U.S. Food and Drug Administration (FDA)
Vaccines
Validation
u.s. Food and Drug Administration Fda
Good Laboratory Practice Glp
Regulatory
Leadership
Sales
Public Speaking
Research and Development R&d
Microsoft Office
Project Management
Marketing
u.s. Food and Drug Administration
Research and Development
Good Laboratory Practice
Marc Wiles Summary
Marc Wiles, based in United States, is currently a Global Head of Regulatory Affairs at JCR Pharmaceuticals. Marc Wiles brings experience from previous roles at Aptose Biosciences, Inc., Agenus, Baxter International Inc. and Camargo Pharmaceutical Services. Marc Wiles holds a 1986 - 1991 PhD in Cell Biology, Microvascular Physiology @ Boston University. With a robust skill set that includes Assay Development, Biochemistry, Biologics, Biopharmaceuticals, Biotechnology and more. Marc Wiles has 1 emails and 3 mobile phone numbers on RocketReach.
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