- Location
- Buenos Aires, Argentina
- Type
- Full-time
- Source
- Workday
Description
We are seeking 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:
Under general guidance, the Quality Control Analyst reviews and ensures adherence to study set-up processes and procedures during study start-up and amendment phases for global clinical research studies. This role performs quality control of laboratory documentation and database configurations, supports process excellence, and helps maintain consistent quality standards across the organization.
What You'll Be Doing:
- Perform quality control reviews of laboratory specifications and related study documentation including LSDs, lab events, testing requirements, blood volume charts, toxicity charts, blinding charts, sponsor standards, and ICS documents
- Review project databases against laboratory specification documents to verify accuracy, completeness, and protocol alignment
- Collaborate with Set-up Managers, Set-up Specialists, and cross-functional teams to resolve quality findings and support study deliverables
- Monitor and facilitate QC timelines to ensure client expectations and standard turnaround times are achieved
- Analyze quality trends and contribute to training initiatives, process improvements, and quality metrics reporting
- Participate in internal and external audits and ensure activities are performed in accordance with ICH E6 Guideline for Good Clinical Practice
- Support the training, mentoring, and development of junior staff and QC team members
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 reviewing project databases, laboratory specifications, and study set-up documentation within a regulated environment
- Other equivalent combination of education, training, and experience may be accepted in lieu of degree
The Knowledge, Skills and Abilities Needed for This Role:
- Understanding of medical and clinical research terminology and knowledge of Set-up Management processes
- Strong organizational, time management, and prioritization skills with the ability to meet strict deadlines in a fast-paced environment
- Excellent written and verbal English communication skills with the ability to build effective relationships with customers, stakeholders, managers, and colleagues
- Strong technical aptitude and attention to detail for document control and quality metrics management
- Ability to collaborate globally 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 IQVIA 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.
Skills
Project Management
