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Lab Animal Manager Jobs in Reno, NV (NOW HIRING)

Veterinarian

Reno, NV

$100K - $110K/yr

... animal and exotic practice in beautiful Reno, NV. Whether you're experienced with exotics or just ... Full in-house lab and digital radiology * Avimark practice management software * Long-tenured team ...

Veterinarian

Reno, NV

$100K - $110K/yr

... animal and exotic practice in beautiful Reno, NV. Whether you're experienced with exotics or just ... Full in-house lab and digital radiology * Avimark practice management software * Long-tenured team ...

Veterinarian

Reno, NV · On-site

$100K - $110K/yr

... animal and exotic practice in beautiful Reno, NV. Whether you're experienced with exotics or just ... Full in-house lab and digital radiology * Avimark practice management software * Long-tenured team ...

Lab Animal Manager information

See Reno, NV salary details

$9

$25

$45

How much do lab animal manager jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for lab animal manager in Reno, NV is $25.17, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $27.79 per hour, depending on experience, location, and employer.

What does a Lab Animal Manager do?

A Lab Animal Manager oversees the daily operations of animal research facilities, ensuring the well-being and care of laboratory animals. Their responsibilities include supervising staff, maintaining compliance with regulations, coordinating animal care and use protocols, and managing facility budgets. They also ensure that all procedures follow ethical guidelines and may assist with training researchers in proper animal handling techniques. The role is essential to supporting scientific research while maintaining high standards of animal welfare.

What are the main challenges a Lab Animal Manager faces in ensuring animal welfare while meeting research objectives?

Lab Animal Managers often balance strict regulatory compliance and the ethical treatment of animals with the needs of researchers who require timely and reliable results. Common challenges include maintaining detailed records, ensuring proper care protocols are followed, and training staff on best practices. Additionally, Lab Animal Managers collaborate closely with veterinarians, researchers, and regulatory bodies, which requires strong communication skills and adaptability. Proactively addressing these challenges helps maintain a healthy research environment and supports scientific integrity.

What are the key skills and qualifications needed to thrive as a Lab Animal Manager, and why are they important?

To thrive as a Lab Animal Manager, you need expertise in laboratory animal care, facility management, and compliance with regulatory standards, typically supported by a bachelor’s degree in animal science or a related field and certifications like AALAS. Familiarity with animal management software, environmental monitoring systems, and health surveillance protocols is essential. Strong leadership, problem-solving abilities, and effective communication skills help you manage teams and coordinate with researchers. These competencies ensure ethical animal care, regulatory compliance, and efficient facility operation in research environments.
What cities near Reno, NV are hiring for Lab Animal Manager jobs? Cities near Reno, NV with the most Lab Animal Manager job openings:
Infographic showing various Lab Animal Manager job openings in Reno, NV as of June 2026, with employment types broken down into 95% Full Time, 3% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $52,362 per year, or $25.2 per hour.
Sample Management Technician I

$19/hr

Other

Medical, Retirement, PTO

Posted 7 days ago


Charles River Laboratories rating

8.2

Company rating: 8.2 out of 10

Based on 90 frontline employees who took The Breakroom Quiz

26th of 71 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

We are seeking a Sample Management Technician I for our Safety Assessment site located in Reno, Nevada.

Perform a wide variety of basic laboratory support tasks. Perform routine maintenance on basic laboratory equipment. Prepare all materials required for reagent receipt and storage. Pull items to meet requests, prepare sample for analysis, and direct specimens to the appropriate area.Compile required documentation and package reagents for shipping. Assist in the maintenance of general laboratory supply inventory and reagents within the Laboratory Sciences group. May work with items of a delicate/hazardous nature (e.g., blood, cells, tissue).

Job Description

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs), Good Clinical Practice Regulations (GCP), and Standard Operating Procedures (SOPs).
Perform all other related duties as assigned.
May generate reports, data, and forms.
Maintain and perform record keeping.
Review data recorded by others for quality control.
May record observations and measurements for basic lab/research tasks.
Perform clerical duties (e.g.: filing, making copies, etc.).
Perform routine laboratory maintenance of lab equipment.
Remove biohazard and recycle waste from lab to appropriate locations for disposal.
Wash and dry laboratory supplies and distribute to appropriate locations within the laboratory.
Label tubes, devices and containers and perform laboratory set-up/clean-up.
Monitor and stock lab supplies in assigned areas.
Help to prepare materials and data for shipment and archiving.
Package biological reagents and ensure accurate completion of all required documentation for the shipment (i.e.: verify shipping lists).
Prepare shipping documentation and assist in preparation of CITES permits as needed. Fax shipping documentation to sponsors as needed.
Prepare domestic and international packages according to applicable guidelines.
Deliver packages to a carrier/shipper as needed.
Handle all details required for shipment of reagents (receiving, storage, inventory and verification) using Study protocol or Sponsor guidance documents.

QUALIFICATIONS:
 Education: High school diploma or General Education Degree (G.E.D.) required.
 Other: Must be detail oriented and have general familiarity with lab procedures. Good verbal and written communication skills required. Basic computer skills; familiarity with Microsoft Office and Excel software. Ability to organize and prioritize work and meet timelines.

The pay range for this position is $19.00 USD per hour. 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.


What Charles River Laboratories employees say

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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