Associate Laboratory Project Set-up Manager
IQVIABuenos Aires, Autonomous City of Buenos Aires, Argentina
Posted May 20, 2026
Full Time
About the Company
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Job Description
We are seeking an Associate Laboratory Project Set-up Manager to join IQVIA Laboratories. The role involves leading the design and launch of clinical research studies, ensuring high-quality study start-up deliverables while coordinating effectively with sponsors, CROs, and internal laboratory teams.
Requirements
- Develop and manage laboratory database design requirements for protocols, amendments, and sponsor-driven changes
- Define and maintain client-specific design standards in alignment with clinical protocols
- Oversee study database configuration and serve as the primary set-up point of contact for internal and external stakeholders
- Collaborate with cross-functional teams during project planning
- Maintain and update project documentation
- Proactively manage scope changes, identify project risks, and implement contingency plans
- Prepare and present study-specific materials at investigator and kick-off meetings
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Tuition Reimbursement