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Salary
≈ $31k – $72k per year (Estimated)
Location
In office (Buenos Aires)
Seniority
Senior · 1+ year exp
Employment
Full-Time

First seen by Alion on Oct 16, 2026. IQVIA scores B on the Alion truth index.

Overview
Company
Impact
Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

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:

Support the setup, configuration, and validation of laboratory databases within Clinical Trial Management Systems, ensuring quality and compliance with study protocols and regulatory standards. This role is ideal for candidates with foundational clinical research knowledge who are looking to grow into sponsor-facing responsibilities and more complex project ownership.

What You'll Be Doing:

  • Configure and support laboratory databases using LIMS/CTMS platforms, ensuring alignment with study protocols and sponsor requirements
  • Assist with study validation and perform low-complexity updates, building toward ownership of more complex setup activities over time
  • Collaborate with cross-functional teams to ensure smooth project setup and timely delivery
  • Maintain accurate documentation and proactively communicate risks, issues, and timeline impacts
  • Participate in project planning, including timelines, regulatory checkpoints, and issue identification

What We Are Looking For:

  • High School Diploma or equivalent required; Bachelor's Degree in Life Sciences or related field preferred
  • Minimum 1 year relevant experience in the Clinical, Medical or Healthcare industry.
  • Experience working with Clinical Trial Management Systems (CTMS), LIMS, or similar laboratory database tools
  • Basic understanding of clinical research processes, including protocol review and study setup
  • Other Equivalent combination of education, training, and experience may be accepted in lieu of degree

The Knowledge, Skills and Abilities Needed for This Role:

  • Strong organizational skills and attention to detail, with ability to manage multiple priorities in a fast-paced environment
  • Ability to work effectively with cross-functional teams and progressively engage with sponsors and stakeholders
  • Interest in innovation, including exposure to AI-enabled tools and process improvement initiatives

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 https://jobs.iqvia.com/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 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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