Clinical Lab Scientist I — Trials & Validation

Roche; Tucson (AZ); On-site; USD 66,000 - 122,000; Full time

Benefits offered by this job

Discretionary annual bonus

Job summary

Roche in Tucson seeks a Lab Scientist Professional to perform high complexity laboratory testing on clinical specimens, evaluating quality control and results against acceptance criteria to inform project decisions.

You will support the laboratory's Clinical Testing Site activities, conduct Clinical Validation testing, document procedures per CFR/ICH guidelines, and ensure timely, accurate records while maintaining safety and regulatory compliance.

Qualifications

• Bachelor’s degree in Biological/Life Sciences, Chemistry, Biochemistry or related field.
• Minimum 2 years of basic laboratory experience.
• Experience documenting clinical trial activities in Case Report Forms, Sample Accountability, and Investigational Material Accountability Logs.
• Ability to work under general supervision and plan own work.
• Ability to multi-task and work with cross-functional teams.

Responsibilities

• Perform high complexity lab testing on clinical specimens.
• Evaluate quality control and test results against acceptance criteria.
• Support Clinical Testing Site by performing Clinical Validation testing.
• Document study protocols and regulatory records per CFR/ICH guidelines.
• Maintain lab safety and ISO/QSR compliance.
• Assist with panel build and sample processing for Clinical Validation Studies.
• Analyze alternative approaches and report to supervisor.

Skills

Attention to detail

Multi-tasking

Collaboration

Problem solving in specialty

Education

Bachelor's degree in Biological/Life Sciences, Chemistry, Biochemistry or related field

Job description

Roche in Tucson seeks a Lab Scientist Professional to perform high complexity laboratory testing on clinical specimens, evaluating quality control and results against acceptance criteria to inform project decisions.

You will support the laboratory's Clinical Testing Site activities, conduct Clinical Validation testing, document procedures per CFR/ICH guidelines, and ensure timely, accurate records while maintaining safety and regulatory compliance.