Senior Laboratory Project Set Up Coordinator

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

Job summary

IQVIA is seeking a dedicated professional to support the setup, configuration, and validation of laboratory databases within CTMS and LIMS platforms in Buenos Aires. You will ensure quality and compliance with study protocols and regulatory standards while growing into sponsor-facing responsibilities.

The role requires a High School Diploma or equivalent, with a Bachelor's in Life Sciences preferred, and at least 1 year in clinical, medical, or healthcare settings.

Qualifications

• 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

Responsibilities

• 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

Education

High School Diploma or equivalent

Bachelor's Degree in Life Sciences

Tools

CTMS

LIMS

Job description

Buenos Aires, Argentina

Full time

R

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 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 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled