Medical Laboratory Technician

Q² Solutions; Santa Clarita (CA); On-site; USD 41,400 - 103,300; Full time

Job summary

A leading laboratory services provider in California is seeking a Medical Laboratory Technician to support clinical trial workflows and ensure data accuracy. This role requires a Bachelor's degree and 2–5 years of experience, with proficiency in programming and strong project management skills. The salary range is competitive, reflecting the critical role in healthcare innovation.

Qualifications

• 2–5 years of relevant work experience.
• Understanding of laboratory data management systems and clinical drug development process.
• Knowledge of FDA, GLP, ICH, ISO HL7 regulations.

Responsibilities

• Test clinical study databases and contribute to project teams.
• Coordinate and execute test cases for laboratory data systems.
• Maintain reusable libraries of test data sets and ensure integrity.

Skills

Functional proficiency in programming languages (SQL, SAS, VGL, SSL, C/C#)

Strong project and task management capabilities

Problem-solving and communication skills

Education

Bachelor's Degree in Computer Science, Life Science, or related field

Equivalent combination of education, training, and experience

Job description

We are seeking Medical Laboratory Technician to join Q2Solutions, IQVIA’s laboratory business at Valencia, CA. Shift: Monday - Friday, 10:00 AM - 6:30 PM

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

This role provides intermediate technical expertise to develop, maintain, and test Laboratory Data Management systems and data extraction tools to support clinical trial workflows and ensure data accuracy for internal and external clients.

What You’ll Be Doing

• Test clinical study databases in alignment with programming standards and validation procedures
• Contribute solutions and insights independently to development and validation project teams
• Coordinate testing plans and execute test cases for laboratory data systems and extractions
• Review specifications for testability and confirm traceability to defined requirements
• Support IT teams in evaluating and implementing new technologies as needed
• Maintain reusable libraries of test data sets and ensure integrity throughout test cycles
• Collaborate across project teams to organize timelines, responsibilities, and deliverables
• Uphold compliance with SOPs, regulatory guidelines, and Good Clinical Practice standards

What We Are Looking For

• Bachelor’s Degree in Computer Science, Life Science, or related field
• 2–5 years of relevant work experience
• Functional proficiency in programming languages such as SQL, SAS, VGL, SSL, and C/C#
• Understanding of laboratory data management systems and the clinical drug development process
• Other Equivalent combination of education, training, and experience may be accepted in lieu of degree

The Knowledge, Skills And Abilities Needed For This Role

• Ability to lift up to 50 lbs, frequent standing and walking, occasional sitting, close eye work requirement (computer, typing, reading small prints). Physical demands vary depending on assigned work area and work tasks. Occasional exposure to cold temperatures.
• Strong project and task management capabilities to meet deadlines and deliverables
• Proficiency in laboratory terminology and regulatory standards including FDA, GLP, ICH, ISO HL7
• Excellent problem-solving and communication skills with a customer-focused mindset

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

The potential base pay range for this role, when annualized, is $41,400.00 - $103,300.00.