Director of Toxicology
$180K - $200K/yr
Directs Scientific Directors, Study Directors and Toxicology Study Operations to ensure high ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
$180K - $200K/yr
Directs Scientific Directors, Study Directors and Toxicology Study Operations to ensure high ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
$180K - $200K/yr
Directs Scientific Directors, Study Directors and Toxicology Study Operations to ensure high ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
Reno, NV · On-site
$210K - $235K/yr
Direct the science and business involved in the conduct, direction and execution of Laboratory ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
Reno, NV · On-site
$210K - $235K/yr
Direct the science and business involved in the conduct, direction and execution of Laboratory ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
... directed by the team lead. • Coordinate the repair of laboratory equipment by outside vendors ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
... directed by the team lead. • Coordinate the repair of laboratory equipment by outside vendors ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
This role functions as an independent Study Director responsible for overseeing the design ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
This role functions as an independent Study Director responsible for overseeing the design ... preclinical drug development with exceptional safety assessment services, state-of-the-art ...
$41.2K - $51.8K
5% of jobs
$51.8K - $62.4K
9% of jobs
$70.4K is the 25th percentile. Wages below this are outliers.
$62.4K - $73K
15% of jobs
$73K - $83.6K
16% of jobs
The median wage is $87.2K / yr.
$83.6K - $94.2K
16% of jobs
$94.2K - $104.8K
14% of jobs
$105.4K is the 75th percentile. Wages above this are outliers.
$104.8K - $115.4K
10% of jobs
$115.4K - $126K
6% of jobs
$126K - $136.6K
4% of jobs
$136.6K - $147.2K
3% of jobs
$147.2K - $157.8K
2% of jobs
$41.2K
$94.1K
$157.8K
A Director of Preclinical Development oversees the early-stage research and testing of drug candidates before they enter clinical trials. They manage preclinical studies, ensuring regulatory compliance, safety, and efficacy assessments. This role involves coordinating with cross-functional teams, external partners, and regulatory agencies to advance promising compounds. Strong expertise in toxicology, pharmacology, and regulatory guidelines is essential. The director plays a key role in shaping the preclinical strategy to support successful drug development.
A Director of Preclinical Development is responsible for overseeing the planning, execution, and management of preclinical research programs, ensuring that studies meet scientific, regulatory, and project milestones. You will typically work with cross-functional teams including toxicologists, pharmacologists, regulatory affairs professionals, and external partners, fostering collaboration throughout the drug development process. The role often involves reviewing study designs and data, preparing regulatory submissions, and providing strategic direction to advance compounds toward clinical testing. Working closely with upper management, you'll play a key part in shaping research priorities and resource allocation. This position offers significant influence over drug development strategies and opportunities for advancement to higher executive or scientific leadership roles.
To thrive as a Director Preclinical Development, you need deep expertise in pharmaceutical or biotechnology research, strong project management abilities, and an advanced degree (Ph.D., Pharm.D., or equivalent) in a life sciences field. Familiarity with regulatory guidelines (such as GLP), experience using data management and statistical analysis software, and prior leadership roles in preclinical studies are essential. Exceptional communication, problem-solving, and team leadership skills set candidates apart in managing multidisciplinary teams and collaborative projects. These competencies are crucial for successfully guiding drug candidates through preclinical stages while ensuring regulatory compliance and timely project delivery.
The most popular types of Preclinical Development jobs in Nevada are:
For Director Preclinical Development jobs in Nevada, the most frequently searched job titles are:
The top searched job categories for Director Preclinical Development jobs in Nevada are:
$180K - $200K/yr
Full-time
Medical, Retirement, PTO
Posted 9 days ago
8.4
Based on 94 frontline employees who took The Breakroom Quiz
22nd of 86 rated pharmaceutical
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 a Director, Toxicology for our Safety Assessment site located in Reno, NV.
Responsible for leading the site toxicology organization, overseeing site toxicology scientific resources, and providing scientific expertise for the site toxicology group. Serves as a member of the Global Toxicology Governance Committee and Site Leadership team. Directs Scientific Directors, Study Directors and Toxicology Study Operations to ensure high scientific quality, protocol adherence, integrity and full GLP compliance of general toxicology studies, as applicable.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
MINIMUM QUALIFICATIONS:
The hiring range for this position in the US is $180,000 - $200,000 yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, location and any collective agreements, if applicable.
About Safety Assessment
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.
About Charles River
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 and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
Get the full story on Breakroom
Sourced by ZipRecruiter
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 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
Scientific research and development services
10,000+ Employees
Wilmington, MA, US
1947