Investigator, Safety Assessment @ GlaxoSmithKline King of Prussia, PA (March 2007 - August 2013)
Reseach Scientist, Study Director - Safety Pharmacology @ (January 2003 - February 2007)
Cellular Electrophysiology Technician @ (January 2001 - January 2003)
Staff Scientist @ (January 2000 - January 2001)
Inhalation Toxicology Technician and Study Director @ Stine-Haskell Research Center (January 1992 - January 2000)
Sealion Trainer and Educator @ (January 1988 - January 1989)
Trainer @ Sealand of Cape Cod (January 1985 - January 1988)
Dwayne Lavoie Education
Bethany College
BS (Biology)
1982-1986
Dwayne Lavoie Skills
Risk Assessment
Drug Development
Animal Models
Toxicology
GLP
In Vivo
Pharmaceutical Industry
Regulatory Submissions
CRO
Assay Development
In Vitro
Lifesciences
Drug Discovery
Pharmaceutics
Sop
FDA
Pharmacology
Clinical Development
IND
Laboratory
Validation
Protocol
Computer System Validation
Pharmacokinetics
Regulatory Requirements
Biomarker Discovery
Biomarkers
HPLC
Bioanalysis
Biopharmaceuticals
Immunology
ADME
Drug Metabolism
High Throughput Screening
Biotechnology
DMPK
Regulatory Affairs
Oncology
Vaccines
Life Sciences
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
CRO Management
Good Laboratory Practice (GLP)
Customer Service
Management
Project Management
Regulatory
Data Analysis
Dwayne Lavoie Summary
Dwayne Lavoie, based in Washington, DC, US, is currently a Toxicologist and Project Manager at Aclairo Pharmaceutical Development Group. Dwayne Lavoie brings experience from previous roles at Aclairo Pharmaceutical Development Group, GSK, GlaxoSmithKline King of Prussia, PA and Bristol-Myers Squibb, Princeton, New Jersey. Dwayne Lavoie holds a 1982 - 1986 BS in Biology @ Bethany College. With a robust skill set that includes Risk Assessment, Drug Development, Animal Models, Toxicology, GLP and more. Dwayne Lavoie has 3 emails and 5 mobile phone numbers on RocketReach.
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