Histologist

Integrated Resources, Inc ( IRI ); Tucson (AZ); On-site; USD 65,000 - 90,000; Full time

Job summary

Integrated Resources, Inc (IRI) in Tucson seeks a laboratory professional to perform high-complexity testing on clinical specimens, interpret results, and report findings in line with CAP/CLIA protocols.

You will work under supervision, plan your own work, and contribute to trials and scientific studies, with focus on IHC/ISH and molecular assays.

Qualifications

• Bachelor's degree in Life Sciences (BA/BS).
• 1-3 years of experience in a clinical lab setting; histology or automated IHC experience preferred.
• Preferred: Histotechnologist certification (HT or HTL).
• Experience with IHC/ISH, chromogenic methods, and molecular assays is a plus.

Responsibilities

• Performs high-complexity testing on clinical specimens and reports results per SOPs and CAP/CLIA guidelines.
• Monitors performance of IHC, ISH, molecular assays and immunoassays; assists with investigations.
• Accessioning of samples and QC of demographic data; communicates with clients on held/rejected samples.
• Maintains safety per SHE/OSHA; participates in routine lab safety inspections.
• Documents results with Good Documentation Practices; supports process improvements.
• May perform basic troubleshooting on instrumentation and contribute to lab maintenance.

Skills

Teamwork

Adaptability

Self-motivation

Communication

Education

Bachelor's degree in Life Sciences

Tools

Ventana Ultra Platform

Job description

***This is a first shift position (9:00 AM to 6:00 PM, M-F)

Job Summary

Responsible for performing high complexity laboratory testing on clinical specimens, interpreting and reporting results and complying with study protocols, Standard Operating Procedures, Test Instructions, and related CAP/CLIA Regulations and guidelines. Participates in scientific studies and activities supporting registrational and non-registrational clinical trials. Receives general instructions; plans and executes own work.

Responsibilities

• Works under general supervision, to support aspects of clinical testing and sample processing, adhering to CAP/CLIA regulations and ISO 15189 guidelines.
• Performs high-complexity testing within the CDx CAP/CLIA Laboratory. Monitors performance of IHC, ISH, molecular assays, and immunoassays; assists with lab failure investigations and root cause analysis.
• Performs accessioning of biological samples (blood, plasma, tissue) and quality control of demographic data input. Communicates with clients on held and rejected samples.
• Performs work according to established internal safety guidelines and procedures, and as specified by appropriate regulatory agencies (SHE, OSHA)
• Critically evaluated quality control and test results against acceptance criteria to support clinical testing.
• Uses technical writing skills and Good Documentation Practices to complete lab documentation, SOPs, and Quality documents.
• Participate in routine lab maintenance and lab safety inspections.
• May perform basic troubleshooting for issues related to instrumentation.
• Analyzes alternative approaches to solve problems or develop new perspectives on existing solutions; initiate and implement process improvements.
• Other duties as assigned by management.

Key Requirements

• Bachelor's degree in Life Sciences (BA/BS)
• 1-3 years of experience in a clinical lab setting; histology or automated IHC experience preferred. Experience with Ventana Ultra Platform is a big plus
• Demonstrates strong teamwork and adaptability, combining a willingness to follow direction with the self-motivation needed to deliver consistent results.
• Preferred: Histotechnologist certification (HT or HTL).
• experience working in a clinical laboratory, Immunohistochemistry (IHC), chromogenic in-situ hybridization (ISH), histology lab experience (CAP/CLIA), immunoassays and molecular biology experience.

The Opportunity

• Lead clinical and medical research studies
• Analyze clinical trial data and publish findings
• Ensure compliance with medical research regulations
• Collaborate with healthcare professionals and research teams
• Support drug and therapy development efforts

Who You Are

• 1-3 years of experience
• Strong problem-solving skills
• Excellent communication abilities
• Knowledge of industry best practices

Preferred (Optional)

Experience in clinical trials preferred.