Laboratory Associate: Clinical Trials Lab Support

IQVIA LLC; Indianapolis (IN); On-site; USD 35,900 - 74,800; Full time

Benefits offered by this job

Benefits package

Career development

Job summary

IQVIA Laboratories in Indiana is seeking a Lab Associate to perform routine testing for clinical trials, following SOPs and regulatory requirements. You will support daily lab operations through specimen analysis, result documentation, and material preparation.

You will collaborate with cross-functional teams, evaluate results against computer-system algorithms, and escalate unusual findings to senior personnel.

Qualifications

• High School Diploma or equivalent required, or a Bachelor's Degree; some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology
• Knowledge of GLP and regulatory standards is needed
• Strong lab safety practices and standard precautions must be followed
• Basic computer skills and familiarity with laboratory instrumentation and terminology
• Ability to communicate clearly and collaborate with internal stakeholders

Responsibilities

• Perform routine analysis of specimens and document results in accordance with SOPs and applicable regulatory guidelines
• Evaluate the validity of analytical results against laboratory computer-system algorithms
• Identify, document, and escalate potential performance errors or unusual results to senior personnel
• Prepare buffers and solutions for analysis and manage post-analysis storage
• Assist with laboratory housekeeping, supply monitoring, and cross-functional communication

Skills

GLP knowledge

Lab safety

Computer skills

Communication

Cross-functional collaboration

Education

Bachelor's Degree

High School Diploma or equivalent

BS in chemistry/biology/medical laboratory technology

Job description

IQVIA Laboratories in Indiana is seeking a Lab Associate to perform routine testing for clinical trials, following SOPs and regulatory requirements. You will support daily lab operations through specimen analysis, result documentation, and material preparation.

You will collaborate with cross-functional teams, evaluate results against computer-system algorithms, and escalate unusual findings to senior personnel.