Research Analyst ; Biologist - Immunology
Listed on 2026-01-01
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Research/Development
Medical Technologist & Lab Technician, Clinical Research -
Healthcare
Medical Technologist & Lab Technician, Clinical Research
Research Analyst I (Biologist) – Immunology
Join Charles River Laboratories as a Research Analyst I (Biologist) in the Immunology team at our Safety Assessment site located in Ashland, OH.
For 75 years Charles River employees have helped discover and develop safe drug therapies. Your work will impact health worldwide.
Job SummaryPerform laboratory tasks, generate and record data, handle samples, and conduct accurate data collection and reporting with minimal supervision.
Essential Duties and Responsibilities- Perform assays such as ELISA, multiplex, immunophenotyping, comet, micronucleus.
- Perform density gradient cell separations.
- May act as lead/primary technician on basic studies.
- Utilize micropipettes for all assays.
- Prepare study materials, order supplies, verify paperwork, label tubes.
- Receive and log reagents, solutions, samples.
- Prepare simple to complex lab solutions.
- Assist in method development, validation, and equipment validations.
- Operate and maintain equipment: microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, eyewash stations.
- Maintain clean work areas.
- Collect and record data in compliance with GLP, SOPs, protocols, study plans.
- Input, print, edit basic to complex data.
- Prepare materials for shipment and archival.
- Review documentation for quality control.
- Perform all other related duties as assigned.
Pay for this position is $21 USD per hour. Starting salaries vary based on factors including experience, skills, education, certifications, and location.
Job Qualifications- Education:
Bachelor’s degree (B.A./B.S.) in a scientific field required. - Experience:
0–2 years related experience in biology, chemistry/pharmacy, or similar lab environment; GLP experience preferred. - Equivalent combination of education and 4 years related experience may be accepted.
- Proficient in basic technical skills and operation of data collection equipment.
- Knowledge of GLPs and federal regulations, basic understanding of study design and protocols.
- Strong teamwork, accurate data recording, verbal and written instruction following, effective communication, professionalism with management, coworkers, and sponsors.
- Quickly learn and utilize computer programs; previous computer experience preferred.
Charles River expedites preclinical drug development with safety assessment services, state‑of‑the‑art facilities, and regulatory guidance.
About Charles RiverWe are a contract research organization providing GLP and non‑GLP services from target identification to preclinical development. With over 20,000 employees in 110 facilities worldwide, we serve global pharmaceutical and biotechnology companies, government agencies, hospitals, and academic institutions.
BenefitsWe offer bonuses/incentives based on performance, 401(k), paid time off, stock purchase program, health and wellness coverage, employee and family wellbeing support programs, and work‑life balance flexibility.
Equal Employment OpportunityCharles 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.
If you need assistance or an accommodation due to a disability, contact our HR team at This email is for accommodation requests only.
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