Toxicology Study Director

Title

Study Director (Dayton, NJ)

Duties Included

  • Supervise preclinical study conduct under OECD, FDA, ICH, EU, ISO etc. regulatory guidelines.
  • Assist in protocol development, design and implementation.
  • Responsibilities as stated in GLP regulations.
  • Data interpretation and report writing.
  • Client liaison.
  • Mentor junior scientists.

Requirements

At least a Bachelor of Science degree or equivalent experience in a field related to their area of responsibility (e.g., toxicology, pharmacology, animal science, chemistry, biology, microbiology, etc.). Advanced degree preferred.

Contact Information

Send resume to:
Dr. Pam Marone
Eurofins | Product Safety Labs
2394 Highway 130, Suite E, Dayton, NJ
PamMarone@Productsafetylabs.com.