Quality Control Analyst – Clinical Research

About the role

IQVIA Laboratories is looking for a Quality Control Analyst to join its Buenos Aires laboratory team. The role ensures the accuracy, quality, and regulatory compliance of study set‑up documentation, databases, and specifications used in clinical research.

Key responsibilities

• Perform quality control reviews of laboratory specifications, study documentation, and associated configuration records.
• Validate project databases against laboratory specification documents to guarantee accuracy and consistency.
• Collaborate with Set‑up Managers, Set‑up Specialists, and cross‑functional stakeholders to resolve quality findings and process issues.
• Coordinate QC activities and timelines to meet client deliverables and standard turnaround expectations.
• Analyze quality trends, support training initiatives, and drive process‑improvement opportunities.
• Maintain quality metrics through document control and accurate error tracking.
• Support audits, mentor new team members, and assist with performance reporting and operational‑excellence projects.

Required profile

• Bachelor’s degree in a science‑related field.
• Minimum 5 years of experience in the clinical or research industry.
• At least 3 years of set‑up or project‑management experience, or an equivalent combination of education and experience.
• Demonstrated proficiency with Microsoft Office, IQVIA systems, and ELVIS.
• Experience working in a regulated environment with knowledge of medical and clinical‑research terminology.

Required skills

• Microsoft Office
• IQVIA systems
• ELVIS

What we offer

• Comprehensive benefits program supporting physical, mental, emotional, and financial wellbeing for employees and their families.
• Opportunities to work on innovative healthcare projects that have a meaningful impact.