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Biotech Research Assistant Jobs in Nevada (NOW HIRING)

... research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate ...

Phlebotomist - Las Vegas

Las Vegas, NV

$16.25 - $20.25/hr

Medical Diagnostic Laboratories (MDL), a member of Genesis Biotechnology Group, is a CLIA certified ... Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis ...

New

Phlebotomist - Las Vegas

Las Vegas, NV

$16.25 - $20.25/hr

Medical Diagnostic Laboratories (MDL), a member of Genesis Biotechnology Group, is a CLIA certified ... Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis ...

New

Phlebotomist - Las Vegas

Las Vegas, NV · On-site

$16.25 - $20.25/hr

Medical Diagnostic Laboratories(MDL), a member of Genesis Biotechnology Group, is a CLIA certified ... Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis ...

New

Phlebotomist - Las Vegas

Las Vegas, NV

$16.25 - $20.25/hr

Medical Diagnostic Laboratories (MDL), a member of Genesis Biotechnology Group, is a CLIA certified ... Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis ...

New

$20 - $60/hr

... software. * Assist with experimental execution, system characterization, troubleshooting, and ... Hands-on academic, research, internship, maker-space, or personal project experience with ...

New

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Showing results 1-20

Biotech Research Assistant information

See Nevada salary details

$8

$22

$32

How much do biotech research assistant jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for biotech research assistant in Nevada is $22.31, according to ZipRecruiter salary data. Most workers in this role earn between $18.85 and $25.96 per hour, depending on experience, location, and employer.

What is a biotech research assistant?

A Biotech Research Assistant supports scientific research by conducting experiments, analyzing data, and maintaining laboratory equipment. They assist in developing new biotechnological products, processes, or medicines. Their responsibilities often include preparing samples, documenting results, and following strict safety protocols. This role requires knowledge of biology, chemistry, and lab techniques, typically obtained through a degree in biotechnology or a related field. Biotech Research Assistants work in academic, pharmaceutical, or industrial labs to advance scientific discoveries.

What are the typical daily responsibilities of a biotech research assistant?

Biotech Research Assistants often spend their days preparing samples, conducting experiments, and performing routine laboratory tests under the supervision of senior scientists. They are responsible for accurately documenting results, maintaining laboratory equipment, and ensuring all procedures follow safety and quality protocols. Collaboration is common, as assistants frequently work closely with other researchers, lab technicians, and sometimes cross-functional teams. This hands-on role provides continuous learning opportunities and is essential in supporting the successful completion of larger research projects.

What are the key skills and qualifications needed to thrive in the biotech research assistant position, and why are they important?

A Biotech Research Assistant typically needs a strong background in biology, chemistry, or a related life science, often supported by a bachelor's degree or equivalent laboratory experience. Familiarity with techniques such as PCR, gel electrophoresis, and experience using laboratory information management systems (LIMS) is highly valued. Attention to detail, strong organizational skills, and the ability to work collaboratively make candidates stand out in this role. These competencies are essential to ensure experiments are conducted accurately, data is reliably recorded, and research projects progress smoothly.

Do biotech research assistants get paid a lot?

Biotech research assistants typically earn a moderate salary that varies based on experience, education, and location. Entry-level positions often pay around $40,000 to $50,000 annually, with potential increases as skills and responsibilities grow. The role may require familiarity with laboratory techniques and data analysis tools, which can influence compensation.

What qualifications do you need to be a biotech research assistant?

A biotech research assistant typically needs at least a bachelor's degree in biology, biotechnology, or a related field. Relevant laboratory skills, familiarity with scientific equipment, and attention to detail are important, and some positions may require experience with data analysis or specific techniques like PCR or cell culture.

What are popular job titles related to Biotech Research Assistant jobs in Nevada?

For Biotech Research Assistant jobs in Nevada, the most frequently searched job titles are:

What cities in Nevada are hiring for Biotech Research Assistant jobs?

Cities in Nevada with the most Biotech Research Assistant job openings:

Infographic showing various Biotech Research Assistant job openings in Nevada as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $46,405 per year, or $22.3 per hour.

$24/hr

Full-time

Medical, Retirement, PTO

Re-posted 8 days ago


Charles River Laboratories rating

8.3

Company rating: 8.3 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

25th 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 Summary

We are seeking a Research Analyst I for our Safety Assessment site located in Reno, NV

This position will be responsible for handling and processing samples and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies.

Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Executes scientific testing strategies and studies. May participate in development as part of team. May lead assay research, assay validation or study conduct, or is involved in preparation of material (e.g. protein, nucleic acid, cells, etc.).

Reviews and interprets study data, communicates results to clients and writes final reports. Ensures compliance with protocols and all applicable SOPs. Troubleshoots and resolves assay or technical issues in the laboratory when scientific expertise is needed. Contributes to specific dataset interpretation, or when appropriate answering questions from regulatory authorities. For singular focus of Chemistry or Biology disciplines, refer to specified role on job architecture.

Job Qualifications

The following are minimum requirements related to the Research Analyst I position.

  • Associate's degree (A.A. / A.S) or equivalent in biological science or related discipline required.  Bachelor’s degree (B.A. / B.S.) preferred. 
  • 6 Months minimum related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Proficient in basic technical skills and the operation of data collection equipment.
  • Knowledge of GLPs and other federal regulations and guidelines.
  • Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information.
  • Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.
  • Able to quickly learn and utilize computer programs as needed.
     

The pay for this position starts at $24/hr.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. 

Schedule: Monday - Friday 8 am - 5 pm (other shifts may be available) 

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 Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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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Benefits

Hours and flexibility

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Get the full story on Breakroom


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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