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Mark Pratt Location
Occitanie, France
Mark Pratt Work
Senior Toxicologist @ (January 2024 - Present)
Scientific Director, Nonclinical Safety Lead @ (April 2018 - October 2023)
Associate Director, Regulatory Consultant (Non-Clinical) @ Syneos Health (Previously INC Research/inVentiv Health) (June 2017 - March 2018)
Associate Director of Non-Clinical Development @ (October 2014 - June 2017)
Non-Clinical Project Lead @ (June 2011 - October 2014)
Toxicologist @ (September 2009 - June 2011)
Toxicologist @ Antisoma (July 2008 - November 2008)
Toxicologist @ (January 2007 - December 2008)
Toxicologist @ (December 2001 - April 2007)
Mark Pratt Education
University of Birmingham
M.Sc (toxicology)
2000-2001
The Manchester Metropolitan University
2:ii (Biomedical Sciences)
1997-2000
Mark Pratt Skills
GLP
ADME
In Vivo
Biomarkers
Toxicology
Pharmacokinetics
CRO
Regulatory Submissions
Drug Development
DMPK
Drug Discovery
Pharmaceutical Industry
Discovery Toxicology
PK/PD
Animal Models
Out-licensing
Pre-clinical Studies
Gastroenterology
Hepatology
Clinical Chemistry
Urinalysis
Hematology
Pathology
Drug Safety
Study Monitoring
Toxicokinetics
Impurities
Histopathology
Pharmaceuticals
ISO 10993
Regulatory Affairs
R&D
Pharmaceutics
In Vitro
Lifesciences
Biopharmaceuticals
Biotechnology
Pharmacology
Immunology
IND
Validation
SQL Server
Licensing
Clinical Data
Out Licensing
Microsoft Office
Customer Service
Management
Pre Clinical Studies
Due Diligence
Hospitals
DBMS
Mark Pratt Summary
Mark Pratt, based in Occitanie, France, is currently a Senior Toxicologist at Pierre Fabre Group. Mark Pratt brings experience from previous roles at The Janssen Pharmaceutical Companies of Johnson & Johnson, Syneos Health (Previously INC Research/inVentiv Health) and Norgine. Mark Pratt holds a 2000 - 2001 M.Sc in toxicology @ University of Birmingham. With a robust skill set that includes GLP, ADME, In Vivo, Biomarkers, Toxicology and more. Mark Pratt has 3 emails on RocketReach.
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