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Phd Animal Science Jobs in Nevada (NOW HIRING)

Phd Animal Science information

See Nevada salary details

$62.9K

$163.8K

How much do phd animal science jobs pay per year?

As of Aug 30, 2026, the average yearly pay for phd animal science in Nevada is $161,903.00, according to ZipRecruiter salary data. Most workers in this role earn between $162,400.00 and $162,400.00 per year, depending on experience, location, and employer.

What is a PhD animal science professional?

PhD Animal Science professionals are experts who have completed a doctoral degree focused on the biology, management, and welfare of animals, often specializing in areas like genetics, nutrition, physiology, or animal behavior. They conduct advanced research, teach at universities, and often contribute to innovations in livestock production, animal health, and sustainable agriculture. These professionals work in academia, government agencies, private industry, or research institutions to solve complex problems related to animal systems and agriculture.

What types of collaborative projects can a PhD animal science professional expect to participate in within academic or industry settings?

PhDs in Animal Science often work closely with multidisciplinary teams, such as veterinarians, nutritionists, geneticists, and farm management professionals. Collaborative projects may include designing and conducting research studies on animal health, welfare, nutrition, or genetics, as well as working with external partners like agricultural companies or government agencies. Regular cross-functional meetings and joint fieldwork are common, requiring strong communication and teamwork skills. These experiences not only advance scientific knowledge but also provide valuable networking and leadership opportunities.

What are the key skills and qualifications needed to thrive as a PhD animal science professional, and why are they important?

To thrive as a PhD in Animal Science, you need advanced knowledge of animal biology, genetics, nutrition, and research methodologies, typically backed by a doctoral degree in animal science or a related field. Expertise with laboratory equipment, statistical analysis software (such as SAS or R), and experience publishing in scientific journals are commonly required. Strong analytical thinking, problem-solving abilities, and effective communication skills help you design studies, interpret data, and share findings with diverse audiences. These competencies are crucial for driving scientific innovation, improving animal welfare, and advancing research in both academic and industry settings.

What is the difference between Phd Animal Science vs Animal Nutritionist?

AspectPhd Animal ScienceAnimal Nutritionist
Required CredentialsDoctoral degree in Animal ScienceBachelor’s or Master’s in Animal Nutrition, often with certification
Work EnvironmentResearch labs, universities, academiaFarms, feed companies, consulting firms
Industry UsageAcademic research, teaching, advanced research rolesPractical nutrition planning, feed formulation, consulting

While both roles focus on animal health and nutrition, a Phd Animal Science typically involves advanced research and academic work, whereas an Animal Nutritionist applies nutritional knowledge directly in practical settings like farms and feed companies. The Phd prepares for research and teaching, while the Nutritionist focuses on practical application and consulting.

What cities in Nevada are hiring for Phd Animal Science jobs?

Cities in Nevada with the most Phd Animal Science job openings:

Infographic showing various Phd Animal Science job openings in Nevada as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, and 2% Contract. Highlights an 74% Physical, 3% Hybrid, and 23% Remote job distribution, with an average salary of $161,903 per year, or $77.8 per hour.

$72K - $88K/yr

Full-time

Medical, Retirement, PTO

Posted yesterday

New


Charles River Laboratories rating

8.4

Company rating: 8.4 out of 10

Based on 94 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical


Job description

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.

JOB OVERVIEW

As a Senior Scientific Associate, you will function as an independent Study Director responsible for leading pre-clinical toxicology and safety assessment studies of basic complexity. You will collaborate cross-functionally and communicate directly with our clients, serving as an important point of coordination throughout the study lifecycle.

This position provides an opportunity to expand scientific, operational, and client-facing experience while building the skills necessary to lead increasingly complex toxicology studies and progress within the Research Scientist/Study Director career path.

ESSENTIAL DUTIES & RESPONSIBILITES

  • Oversee preclinical toxicology and safety assessment studies of basic complexity.
  • Oversee study conduct from protocol development through final reporting, ensuring studies are executed in accordance with applicable regulatory requirements and Good Laboratory Practice (GLP) standards.
  • Design, review, and maintain study plans, amendments, schedules, and other study-related documentation.
  • Coordinate study activities across scientific, veterinary, laboratory, and operational teams to ensure successful study execution.
  • Interpret study data and contribute to the preparation, review, and delivery of scientific reports.
  • Serve as a point of contact for clients, participating in study-related meetings, teleconferences, site visits, and ongoing communications.
  • Develop a strong understanding of study management, study budgets, and the operational factors that influence successful study delivery.
    Collaborate with experienced Toxicology leaders to develop the scientific, operational, and client-facing skills required for increasingly complex Study Director responsibilities.
  • Interact closely with Quality Assurance, veterinary, and technical teams while building expertise in regulatory compliance, animal welfare, and study oversight processes.
  • Contribute to departmental initiatives, continuous improvement efforts, and the ongoing growth of the Toxicology organization.

Required Qualifications

  • Bachelor's degree in Toxicology, Biology, Pharmacology, Animal Science, Veterinary Science, Life Sciences, or related scientific discipline.
  • Minimum of 5 years of relevant experience, or an equivalent combination of education and experience.
  • Experience working in a regulated scientific, laboratory, research, or preclinical environment.
  • Strong organizational, communication, and collaboration skills.
  • Demonstrated ability to manage multiple priorities and work effectively across functional teams.

Preferred Qualifications

  • Advanced degree (MS, PhD, DVM, PharmD, or related discipline).
  • Experience supporting nonclinical safety assessment, toxicology, pathology, necropsy, clinical pathology, technical operations, or related scientific programs.
  • Experience working directly with Study Directors or supporting regulated studies.
  • Previous leadership, team lead, supervisory, or project coordination experience.
  • Experience interacting with internal stakeholders and/or external clients.

The pay range for this position is $72K-$88K annually.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

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.


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About Charles River

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.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947