Research Analyst I - Immunology

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 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.

Qualifications

• 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.
• 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.