Experience

Actinium Pharmaceuticals, Inc.

• United States
• Biotechnology Research
• 1 - 100 Employee

• Associate Director Preclinical Toxicology

  • Oct 2022 - Present



Kadmon, a Sanofi Company

• United States
• Biotechnology Research
• 1 - 100 Employee

• Associate Director, Nonclinical Development

  • Sep 2019 - Oct 2022

  New York, NY, United States



PsychoGenics

• Sr. Research Associate

  • Oct 2008 - Oct 2019

• Associate Scientist

  • Oct 2008 - Oct 2019

  New Jersey -Coordinate, plan, and manage studies with sponsor study directors. Draft SOPs, and IACUC amendments. -Analyze data and prepare reports for clients. -Conduct surgical procedures for self -administration studies, pain studies, traumatic brain injury and oncology studies. -Xenotransplantation of human cancer cells into mice. -Conduct PK study endpoints, blood/plasma/serum/CSF collection, tissue harvesting (brain, CNS, kidney), tumor measurement, bleeds, and profusions.… Show more -Coordinate, plan, and manage studies with sponsor study directors. Draft SOPs, and IACUC amendments. -Analyze data and prepare reports for clients. -Conduct surgical procedures for self -administration studies, pain studies, traumatic brain injury and oncology studies. -Xenotransplantation of human cancer cells into mice. -Conduct PK study endpoints, blood/plasma/serum/CSF collection, tissue harvesting (brain, CNS, kidney), tumor measurement, bleeds, and profusions. -Validate novel in vivo models. -Maintain compliance with company SOPs as well as IACUC, AAALAC, and DEA protocols regarding animal welfare and handling chemical compounds. -Train group members to run behavioral tests, perform basic pharmacology practices, and dose mice and rats. -Conduct extensive literature reviews to assist in the design of new or more optimized experimental protocols. -Spearhead, optimize, and pilot new projects that directly led to a new assay product offerings, boosting revenue through additional contracts from old clients as well as attracting new clients.



Sanofi

• France
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Assistant Scientist

  • Apr 2005 - Aug 2008

  Bridgewater, N.J. Study director/Principal Investigator for long term Oncology studies Design and manage toxicology research under Good Laboratory Practices (GLP) regulations for studies which consist of daily dosing and clinical signs for lab mice, rats, dogs, and, rabbits. Perform necropsies for tissue collections at end of study as well as to investigate early cause of deaths. Organize data and prepare reports for FDA approval.



Rutgers University

• United States
• Higher Education
• 700 & Above Employee

• Laboratory Assistant

  • Jun 2004 - Apr 2005

  New Brunswick, N.J. Susan L Cullman Laboratory for Cancer Research Daily husbandry and dosing of lab mice, rats. Breeding of nude transgenic mice for oncology studies. Monitoring and measuring of tumors on nude mice.