Principal Clinical Product Risk Specialist @ (January 2019 - November 2025)
Principal Preclinical Research Associate, Research and Technology Center (RTC) @ (August 2015 - December 2018)
Associate Scientific Director @ (January 2014 - August 2015)
Senior Scientist and Operations Manager @ (January 2010 - January 2014)
Scientist @ (January 2008 - January 2010)
Senior Study Director @ (February 2008 - July 2008)
Senior Preclinical Research Associate @ (January 2006 - January 2008)
Advanced Pharmacologist @ (January 2004 - January 2006)
Advanced Toxicologist and Toxicologist (1998-2004) @ (January 2000 - January 2004)
Scientist @ (January 1996 - January 1998)
Senior Laboratory Technician @ National Reparative Medicine Foundation (January 1994 - January 1996)
Mark Lisowski Education
University of Minnesota Duluth
Bachelor's Degree (Cell Biology and Anatomy)
1988-1992
Mark Lisowski Skills
Laboratory
Immunoassays
Clinical Trials
CRO
ELISA
In Vivo
HPLC
Animal Models
Clinical Research
Biotechnology
Immunology
Life Sciences
Cell Culture
Validation
Medical Devices
Drug Discovery
Molecular Biology
Lifesciences
Drug Delivery
Protocol
Immunohistochemistry
Clinical Development
In Vitro
Regulatory Submissions
Microbiology
Pharmacology
Science
GLP
Toxicology
R&D
FDA
IND
Pharmacokinetics
Mark Lisowski Summary
Mark Lisowski, based in Wisconsin, United States, is currently a Technical Writing Supervisor and Senior Technical Writer at NAMSA. Mark Lisowski brings experience from previous roles at Boston Scientific, Surpass, Inc and Surpass. Mark Lisowski holds a 1988 - 1992 Bachelor's Degree in Cell Biology and Anatomy @ University of Minnesota Duluth. With a robust skill set that includes Laboratory, Immunoassays, Clinical Trials, CRO, ELISA and more. Mark Lisowski has 1 emails and 3 mobile phone numbers on RocketReach.
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