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Biotech Research Analyst Jobs in Michigan (NOW HIRING)

Interpret and perform complex data analysis on experimental results and determine whether they are ... biotechnology industries. * Train and mentor students and lab staff. Required Qualifications*

The Zifo Lab Computing Analyst provides technical laboratory services, including multivendor ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

The Zifo Lab Computing Analyst provides technical laboratory services, including multivendor ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

The Zifo Lab Computing Analyst provides technical laboratory services, including multivendor ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

The Zifo Lab Computing Analyst provides technical laboratory services, including multivendor ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Job Summary : Global Pharma Tek is seeking a System Analyst to ensure digital accessibility ... Research Organisation that provides End-to-End Services in Pharma, Biotech and Medical Device ...

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Showing results 1-20

Biotech Research Analyst information

See Michigan salary details

$26.8K

$58.8K

$90.8K

How much do biotech research analyst jobs pay per year?

As of Sep 12, 2026, the average yearly pay for biotech research analyst in Michigan is $58,753.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,800.00 and $64,500.00 per year, depending on experience, location, and employer.

What is a biotech research analyst?

A Biotech Research Analyst is a professional who evaluates companies, products, and trends within the biotechnology sector, often for investment or business strategy purposes. They analyze scientific data, clinical trial results, and market trends to assess the potential of biotech products and companies. Their work helps inform decisions for investors, pharmaceutical firms, and other stakeholders. Biotech Research Analysts typically have a background in life sciences and strong analytical skills.

What are the key skills and qualifications needed to thrive as a biotech research analyst, and why are they important?

To thrive as a Biotech Research Analyst, you need a strong background in biology or biotechnology, analytical skills, and typically a bachelor's or master's degree in a related field. Familiarity with laboratory techniques, data analysis software (like R or Python), and experience using scientific databases are commonly required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills are vital for conducting accurate research, interpreting complex data, and contributing valuable insights to scientific and business objectives.

What are some common challenges faced by biotech research analysts when interpreting experimental data?

Biotech Research Analysts often encounter challenges in interpreting experimental data due to the complexity and variability inherent in biological systems. Ensuring data accuracy, controlling for confounding variables, and distinguishing meaningful trends from background noise require strong analytical skills and attention to detail. Collaborating closely with scientists and statisticians is essential to validate findings and refine experimental methodologies. Staying updated on the latest data analysis tools and industry best practices can help address these challenges effectively.

What is the difference between Biotech Research Analyst vs Biotech Laboratory Technician?

AspectBiotech Research AnalystBiotech Laboratory Technician
Required CredentialsBachelor's or Master's in Biology, Biotechnology, or related field; some roles may require certificationsAssociate's degree or relevant technical certification; laboratory training
Work EnvironmentOffice-based, data analysis, report writing, and project planningLaboratory setting, conducting experiments and sample testing
Employer & Industry UsagePharmaceutical companies, biotech firms, research institutionsResearch labs, hospitals, biotech manufacturing facilities

Biotech Research Analysts focus on analyzing data, interpreting research results, and preparing reports, often working in office environments. In contrast, Biotech Laboratory Technicians perform hands-on laboratory work, conducting experiments and managing samples. Both roles are essential in biotech research but differ in daily tasks, required credentials, and work settings.

What cities in Michigan are hiring for Biotech Research Analyst jobs?

Cities in Michigan with the most Biotech Research Analyst job openings:

Infographic showing various Biotech Research Analyst job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 18% Part Time, and 1% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $58,753 per year, or $28.2 per hour.

Research Analyst I

Mattawan, MI • On-site

Charles River Laboratories, Inc.
Scientific Research and Development Services • 10K+ employees

$23.50/hr

Full-time

Medical, Retirement, PTO

Re-posted 9 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


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

The Immunotoxicology group supports the safety assessment of preclinical treatments and procedures as well as clinical sample analysis using cell based assays including primarily flow cytometry and ELISpot, cell culture and cell isolation, and plate based assays.  An array of platforms and instruments are used to support these assays that include BD LSR Fortessa and Cytek Aurora flow cytometers for traditional and spectral cytometry, FCS Express for immunophenotyping analysis, and the ImmunoSpot analyzer for ELISpot.  Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine samples analysis in both the regulated and non-regulated space of non-clinical and clinical studies.

Essential Functions:

  • Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
  • Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
  • Assist with laboratory maintenance functions
  • Independently perform laboratory support functions such as labeling and solution preparations
  • Assist with maintaining study specific inventory of consumables with oversight
  • Write both study and non-study deviations with minimal oversight
  • Actively participate in process improvement initiatives with oversight
  • Develop critical thinking, troubleshooting and time management skills aligned with needs of the operational area
  • Assist in execution of routine sample analysis studies with oversight
  • Assist in execution of method validation projects with oversight as needed
  • Operate laboratory instruments with complete oversight
  • Assist with data analysis in appropriate software for at least one analytical platform
  • Performs all other related duties as assigned 
Job Description

Job Qualifications:

  • Minimum of a Bachelor's degree (BA/BS) in a science related field.
  • Ability to communicate verbally and in writing at all levels inside and outside the organization
  • Basic familiarity with Microsoft Office Suite
  • Computer skills, commensurate with Essential Functions, including the ability to learn validated systems, ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
  • Ability to work under specific time constraints
  • Ability to work on an 'on-call' as needed on a rotational basis
  • Must be authorized to work in the United States without a sponsor visa, now or in the future.
     
     
    The pay rate for this position is $23.50/hour.
Education
No degree required
Physical Requirements

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