2012 -2014 Director and General Manager @ ERA Consulting (UK) Ltd.
2011 -2012 Sr. Vice President, Operations @
2009 -2010 Head of Toxicology @
2007 -2008 Sr. Director, Nonclinical Development @ Shire HGT
2004 -2007 Sr. Director Preclinica and Nonclinical R and D @
1995 -2004 Sr. Cell Biologist and Molecular Pharmacologist to Director Cell Biology and Principle Investigator @ NeXstar / Gilead / OSI Pharmaceuticals
now Post-Doc @ Parke-Davis
Marc Wiles Education
Boston University
PhD (Cell Biology, Microvascular Physiology)
1986-1991
Macalester College
BA (Biology, Chemistry - Highest Honors)
1982-1986
Marc Wiles Skills
Pharmacology
Pharmaceutical Industry
Drug Development
Clinical Development
Cell
Oncology
Protein Chemistry
Pharmacokinetics
Toxicology
Cell Biology
Lifesciences
Biopharmaceuticals
Regulatory Affairs
Regulatory Submissions
GMP
Drug Discovery
R&D
Biotechnology
Technology Transfer
Molecular Biology
IND
GLP
In Vitro
Validation
Vaccines
FDA
Drug Delivery
CRO
Immunoassays
ELISA
Cell Culture
In Vivo
Biochemistry
Life Sciences
u.s. Food and Drug Administration Fda
Biologics
Good Laboratory Practice Glp
Regulatory
Leadership
Sales
Public Speaking
CRO Management
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 Pharmacology, Pharmaceutical Industry, Drug Development, Clinical Development, Cell and more. Marc Wiles has 1 emails and 3 mobile phone numbers on RocketReach.
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