Laboratory Associate

IQVIA

United States

On-site

USD 36,000 - 75,000

Full time

14 days+

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Job summary

IQVIA Laboratories in Durham is seeking a Lab Associate to join our team. You will perform routine laboratory testing procedures to generate data used in clinical trials research, following SOPs and regulatory requirements.

You will support daily lab operations through specimen analysis, result documentation, material preparation, and collaboration with cross-functional stakeholders, while adhering to GLP and safety standards.

Qualifications

  • 6 months relevant lab experience or equivalent mix of education and training
  • Basic knowledge of GLP and regulatory standards
  • Knowledge of lab safety and infection control procedures

Responsibilities

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

Skills

GLP knowledge
Laboratory safety
Communication skills

Education

High School Diploma or equivalent; or Bachelor's Degree
BS in chemistry, biology, or medical laboratory technology (optional)

Tools

Laboratory equipment operation
Computer basics

Job description

We are seeking a Lab Associate to join IQVIA Laboratories in Durham.

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.

Job Summary:

Perform routine laboratory testing procedures to generate data used in clinical trials research while following SOPs and applicable regulatory requirements. Support daily lab operations through specimen analysis, result documentation, material preparation, and collaboration with cross-functional stakeholders.

What You’ll Be Doing:
  • Perform routine analysis of specimens and document results in accordance with SOPs and applicable regulatory guidelines
  • Evaluate the validity of analytical results against algorithms displayed by the laboratory computer system
  • Identify, document, and escalate potential performance errors or unusual results to senior laboratory personnel
  • Prepare buffers and solutions required for analysis and manage post-analysis sample and reagent storage
  • Assist with laboratory housekeeping, supply monitoring, and communication with cross-functional stakeholders
What We Are Looking For:
  • 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
  • 6 months relevant lab experience Req Or Equivalent combination of education, training and experience Req
  • Basic knowledge of Good Laboratory Practices (GLP) and applicable regulatory agency standards
  • Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling
  • 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 maintain effective reporting procedures and control workflow
  • Ability to effectively collaborate with internal stakeholders and communicate clearly, accurately, and in a timely manner
  • Basic computer skills and knowledge of laboratory equipment, instrumentation, and terminology used in the area of responsibility
What We Offer You:

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. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

To learn more about our benefits, visit IQVIA Benefits.

If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $35,900.00 - $74,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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