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Research Analyst ; Biologist - Immunology

Job in Ashland, Ashland County, Ohio, 44805, USA
Listing for: Charles River
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Medical Technologist & Lab Technician, Clinical Research
  • Research/Development
    Medical Technologist & Lab Technician, Clinical Research
Salary/Wage Range or Industry Benchmark: 21 USD Hourly USD 21.00 HOUR
Job Description & How to Apply Below
Position: Research Analyst I (Biologist) - Immunology

Research Analyst I (Biologist) - Immunology

Location:

Ashland, OH, US, 44805

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 Immunology team at our Safety Assessment site located in Ashland, OH.

Basic Summary

Perform laboratory tasks by various basic methods. Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting.

Essential Duties and Responsibilities
  • Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus.
  • Perform density gradient cell separations.
  • May act as a lead/primary technician on basic studies.
  • Utilize micropipettes for all assays.
  • Perform study preparation activities including ordering supplies, preparing/verifying paperwork, and tube labeling.
  • Receive and log reagents, solutions, and samples.
  • Prepare simple to complex lab solutions.
  • Assist in method development studies, method validation studies, and equipment validations as needed.
  • Operate, perform quality control and maintenance procedures on equipment such as microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, and eyewash stations.
  • Maintain clean work areas by cleaning dishes/glassware, wiping down countertops, and sweeping/mopping floor as needed.
  • Collect and record data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), protocols, and study plans.
  • Input, print, and edit basic to complex data.
  • Prepare materials for shipment and archival.
  • Review documentation for quality control.
  • Perform all other related duties as assigned.

The pay for this position is $21 USD per hour. Please note that starting salaries vary based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications
  • Education:

    Bachelor’s degree (B.A./B.S.) in a scientific field required.
  • Experience:

    Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment. GLP experience preferred.
  • An equivalent combination of education and four years related experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Certification/Licensure:
    None.
  • Other:
    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; previous computer experience preferred.
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…

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