For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary
We are seeking an experienced Research Scientist 2, Toxicology
for our Safety Assessment
site located in Reno, Nevada
The Research Scientist 2, Toxicology
will for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned. The Research Scientist 2, Toxicology
would be responsible for protocols/study plans, coordinates with technical teams to allow appropriate execution of the study, including establishing study schedules, ensuring adequate Standard Operating Procedures are available and adhered to, oversees adequate data recording and reporting, and ensures regulatory requirements/expectations are met for the assigned study(ies). This individual would also function as an independent Study Director in accordance with the applicable Good Laboratory Practices (GLPs). Job Qualifications
The following are minimum requirements related to the Research Scientist 2, Toxicology
About Safety Assessment
- Bachelor's (BA/BSc), Master's (MA/MSc), Doctorate (PhD), PharmD, DVM, or MD degree or equivalent in Toxicology, Pharmacology, or a related discipline.
- Generally 5 to 8 years related industry experience.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. May represent an entry level for individual with relevant Doctorate (PhD), PharmD, DVM, or MD degree or equivalent in Toxicology, Pharmacology, or a related discipline.
- Certification/Licensure: None
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.