Project Services Lab Quality Control Analyst

IQVIA; Buenos Aires; On-site; ARS 1,200,000 - 1,800,000; Full time

Job summary

IQVIA Laboratories in Buenos Aires seeks a Project Services Lab Quality Control Analyst to ensure accuracy, quality, and compliance of study setup documentation, databases, and specifications for clinical research.

The role partners cross-functionally to identify quality improvements, maintain metrics, and support global quality standards in line with ICH E6 Good Clinical Practice guidelines. Strong organizational and communication skills are essential.

Qualifications

• Bachelor’s Degree in a Science related field.
• 5 years’ of clinical or research industry experience.
• 3 year’s Set-up related and/or Project Management experience or Equivalent combination of education, training and experience
• Demonstrated computer proficiency with Microsoft Office, IQVIA systems and ELVIS
• Experience working in a regulated environment with knowledge of medical and clinical research terminology
• Other equivalent combination of education, training, and experience may be accepted in lieu of degree

Responsibilities

• Perform quality control reviews of laboratory specifications, study documentation, and associated configuration records
• Review project databases against laboratory specification documents to ensure 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 support client deliverables and standard turnaround expectations
• Analyze quality trends and contribute to training initiatives and process improvement opportunities
• Maintain quality metrics through document control and accurate error tracking
• Support audits, mentoring activities, and training of new team members
• Assist with performance reporting and special assignments related to operational excellence

Skills

Quality control

Project management

Documentation

Communication

English proficiency

Education

Bachelor's degree in Science

Tools

Microsoft Office

IQVIA systems

ELVIS

Job description

We are seeking Project Services Lab Quality Control Analyst to join IQVIA Laboratories at Buenos Aires, Argentina.

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:

The Quality Control Analyst is responsible for ensuring the accuracy, quality, and compliance of laboratory study set-up documentation, databases, and specifications used in clinical research. This role partners cross-functionally to identify quality improvements, maintain quality metrics, and support consistent global quality standards in accordance with ICH E6 Good Clinical Practice guidelines.

What You’ll Be Doing:

• Perform quality control reviews of laboratory specifications, study documentation, and associated configuration records
• Review project databases against laboratory specification documents to ensure 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 support client deliverables and standard turnaround expectations
• Analyze quality trends and contribute to training initiatives and process improvement opportunities
• Maintain quality metrics through document control and accurate error tracking
• Support audits, mentoring activities, and training of new team members
• Assist with performance reporting and special assignments related to operational excellence
  

What We Are Looking For:

• Bachelor’s Degree in a Science related field
• 5 years’ of clinical or research industry experience
• 3 year’s Set-up related and/or Project Management experience or Equivalent combination of education, training and experience
• Demonstrated computer proficiency with Microsoft Office, IQVIA systems and ELVIS
• Experience working in a regulated environment with knowledge of medical and clinical research terminology
• 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 technical aptitude with knowledge of study set-up management processes, terminology, and quality control practices
• Excellent organizational, time management, communication, and priority-setting skills in a deadline-driven environment
• Ability to build effective working relationships with customers, co-workers, managers, and key stakeholders while maintaining high quality standards
• Strong written and verbal English language communication skills
• Ability to identify quality trends and contribute to continuous 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 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.