Research Scientist I, Toxicology
Listed on 2026-08-02
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Research/Development
Research Scientist, Clinical Research, Medical Science -
Healthcare
Clinical Research, Medical Science
For 75 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.
We are seeking an experienced Research Scientist I for our Safety Assessment site located in Reno, NV.
ResponsibilitiesThe main responsibilities of the Research Scientist I will be to design and/or execute toxicology testing strategies and studies. Other responsibilities of this position include:
- Provides guidance to Sponsors regarding study design and study endpoints.
- Writes study protocols and plans.
- Leads and is responsible for all aspects of the study including in-life, data review and interpretation, communication of results to Sponsors, study updates to the Sponsor, and the draft and final reports.
- Ensures that all Principal Investigators, Individual Scientists, and all key study personnel are held accountable for the various study components.
- Ensures compliance with protocols/study plans, applicable SOPs and BOPs, and regulatory guidance documents.
- Troubleshoots and resolves study issues. Provides advisory functions to clients designing a program or experiment, dealing with specific dataset interpretation, or when appropriate answering questions from regulatory authorities.
The pay range for this position starts at $95,000.00 USD per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
Qualifications AndMinimum Requirements
- Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or Ph.D./D.V.M. preferred.
- Minimum of 6 years related experience in the contract research, academic, or pharmaceutical industry.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
- Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate.
- Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines.
- Proficiency in the use of standard software including Microsoft® Excel, Word, Powerpoint, etc. and with standard laboratory calculations.
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.
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities.
Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources…
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