Research Analyst - Immunology

Job Overview

We are seeking a Research Analyst I - for our Immunology team at our Safety Assessment site located in Ashland, OH.

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.

• Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus.
• Perform density gradient cell separations.
• May act 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 in 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.

• Education:
  
  Bachelor’s degree (B.A/B.S.) in 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 4 years related experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure:
  None
• Must be authorized to work in United States without a sponsor visa now or in the future.
• 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.

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.

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…