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Clinical Trial Material Technician

IQVIA

Clinical Trial Material Technician

full-timePosted: Aug 28, 2026Updated: Sep 1, 2026United States of America, Georgia, Marietta

Job Description

We are seeking a Clinical Trial Material Technician to join IQVIA Laboratories at Marietta, GA.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:As a Clinical Trial Material Technician, you will assemble laboratory test kits that enable investigators to collect data from clinical trial participants. You will perform work in accordance with the ICH E6 Guideline for Good Clinical Practice while supporting accurate, timely study start-up and resupply activities. What You'll Be Doing:Assemble test kits with specimen collection materials as required by protocolPrepare investigator instruction manuals and flowchartsPackage completed test kits, required documentation, return shipping materials, and bulk supplies for shipment to investigatorsPrepare packages for shippingMonitor supply levels and advise your supervisor when inventory falls below required levelsSupport study start-up and resupply requirements by helping prevent supply-related delaysMaintain a clean and orderly work area What We Are Looking For:High School Diploma or equivalent required1 year relevant experience . Equivalent combination of education, training and experience.Experience assembling laboratory test kits with specimen collection materials according to protocolAbility to package clinical trial materials, required documentation, return shipping materials, and ancillary supplies for investigator shipmentBasic computer skillsOther Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:Strong attention to detailGood reading abilityExcellent organizational skillsAbility to establish and maintain effective working relationships with coworkers, managers, and clientsCommitment to maintaining a clean, orderly, and compliant work areaAbility 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. 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.comIQVIA 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. https://jobs.iqvia.com/eoeIQVIA 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 $ 26.800,00 - $ 55.900,00. 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.

Locations

  • United States of America, Georgia, Marietta

Responsibilities

  • Assemble test kits with specimen collection materials as required by protocol
  • Prepare investigator instruction manuals and flowcharts
  • Package completed test kits, required documentation, return shipping materials, and bulk supplies for shipment to investigators
  • Prepare packages for shipping
  • Monitor supply levels and advise your supervisor when inventory falls below required levels
  • Support study start-up and resupply requirements by helping prevent supply-related delays
  • Maintain a clean and orderly work area

Benefits

  • general: 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
  • general: 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. https://jobs.iqvia.com/eoe
  • general: 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.

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