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IQVIA

Runs drug trials and sells health data to pharma

Medical Laboratory Scientist

Diagnostics & Laboratory ProfessionalsConfirmed live in the last 24 hours
Full-timeFairfax, VA, USA$46.2k - $96.2k /yrIn-person

About the Job

Requirements

  • A bachelor's degree in Medical Laboratory Science, Biology, Chemistry, or a related field.
  • Zero to five years of clinical laboratory experience.
  • Meet CLIA requirements for high-complexity testing personnel.
  • Hold national certification as MLS/MT (ASCP, AMT, or equivalent).
  • Have a strong understanding of laboratory principles, testing methodologies, and regulatory standards.
  • Be proficient in laboratory safety, infection control, and handling hazardous chemicals.
  • Be able to perform complex calculations, including averages, standard deviations, and quality control metrics.
  • Be skilled in troubleshooting laboratory instruments and resolving testing issues.
  • Be proficient with Microsoft Excel, Word, and PowerPoint.
  • Be able to manage multiple tasks accurately and with attention to detail.
  • Be able to work effectively with colleagues, management, and external partners.

Responsibilities

  • Perform and report high-complexity laboratory tests, both automated and manual, with minimal supervision.
  • Demonstrate competency in laboratory principles, methodologies, and instrumentation across assigned testing areas.
  • Maintain adequate inventory of reagents and supplies and prepare reagents as required.
  • Identify and report irregularities, instrument issues, or factors that may affect test accuracy.
  • Participate in assay validation, method improvements, and implementation of new technologies.
  • Follow safety procedures, use required personal protective equipment, and report safety concerns.
  • Ensure compliance with CLIA, CAP, GCLP, and internal quality management systems.
  • Adhere to quality control policies, document quality control activities, and maintain a clean, organized work environment.
  • Maintain required training, competency assessments, and continuing education.
  • Support internal and external audits, inspections, and quality initiatives.
  • Verify quality control results and release patient or study results in accordance with regulatory requirements.
  • Assist with training and onboarding laboratory personnel as needed.
  • Perform duties in alignment with ICH E6 Good Clinical Practice guidelines when supporting clinical trials.
  • Participate in special projects and perform additional tasks assigned by laboratory leadership.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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