Research Laboratory Technician

IQVIA

Fairfax (VA)

On-site

USD 43,000 - 89,000

Full time

14 days+

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Job summary

IQVIA in Fairfax, VA is seeking a Research Laboratory Technician to perform routine analysis and laboratory testing procedures for clinical trials. The role requires handling diverse samples, data entry, and inventory management in a busy lab environment.

The position is full-time, on-site in Fairfax, with training on IATA Dangerous Goods and strong emphasis on accuracy and safety in sample processing and documentation.

Qualifications

  • Bachelor’s degree in the sciences is required.
  • 1 year of lab, sample processing and shipping experience preferred but not required.
  • IATA Dangerous Goods handling training will be provided after hire.
  • Proficiency with Word, Excel and databases is expected.

Responsibilities

  • Label, receive, and process samples for clinical trials per protocol guidelines.
  • Request and receive tissue samples from outside pathology facilities.
  • Ship tissue blocks to vendors and slides to the study lab.
  • Record data in forms (paper/electronic) with accuracy.
  • Enter data into departmental database and reconcile discrepancies.
  • Organize and store reagents; maintain a clean lab environment.
  • Restock lab consumables and manage inventory of supplies.
  • Perform administrative tasks: filing, scanning, copying, emailing.

Skills

IATA Dangerous Goods handling
MS Word & Excel

Education

Bachelor’s degree in the Sciences

Job description

Fairfax, VA, United States of America

Full time

Location

On-site in Fairfax, VA

Job Summary

The Research Laboratory Technician is responsible for performing routine analysis and laboratory testing procedures.

Essential Duties and Responsibilities
  • Label, receive, and process samples (blood, urine, tissue, stool, etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department.
  • Request and receive tissue samples from outside pathology facilities.
  • Send tissue blocks to vendor to have slides cut and ship these slides to the study’s lab.
  • Label, receive, and process samples (blood, urine, tissue etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department.
  • Record all data in specified forms per clinical trial (paper and electronic) with accuracy and responsibility.
  • Enter data into departmental database.
  • Recognize discrepancies in the data on the samples and coordinate with the clinical staff to correct.
  • Organize and store all reagents according to safety instructions.
  • Maintain equipment and a clean and orderly lab environment.
  • Restock lab consumables at the end of the day.
  • Manage inventory of clinical trial supplies and kits as well as departmental supplies.
  • Administrative functions include filing, scanning, copying, and emailing of work documents.
  • Ship or store samples as per protocol before the end of the shift.
  • Prepare all collection tubes and aliquots for the next day’s clinic with accuracy and responsibility.
  • Other duties as assigned.
Knowledge, Skills and Abilities
  • IATA Dangerous Goods handling—if not previously certified will train after hire.
  • Comfortable using Microsoft Word and Excel and databases.
Required Education and Experience
  • Bachelor’s degree in the Sciences required.
  • 1 year of prior lab and sample processing and shipping experience preferred but not required.
Why Join Us?

At NEXT Oncology (an Avacare Business), you’ll be part of a mission-driven team that values collaboration, precision, and patient safety. Our team is known for its supportive culture, strong communication, and commitment to excellence in clinical research.

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

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 $42,700.00 - $89,000.00. 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

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