Senior Laboratory Project Set Up Coordinator

IQVIA; Tandil; Presencial; ARS 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

IQVIA in Argentina is seeking a detail-oriented professional to support the setup and validation of laboratory databases within CTMS/LIMS systems, ensuring compliance with study protocols. This entry role offers growth toward sponsor-facing responsibilities and larger project ownership.

You will collaborate with cross-functional teams, maintain documentation, and contribute to planning, timelines, and regulatory checkpoints as you gain more complex ownership over setup activities.

Formación

• High School Diploma or equivalent; Life Sciences degree preferred.
• 1 year minimum relevant experience in Clinical/Medical/Healthcare.
• Experience with CTMS, LIMS or similar laboratory databases.
• Fundamental understanding of clinical research processes and study setup.
• Equivalent education/experience may be considered.

Responsabilidades

• Configure and support laboratory databases using CTMS/LIMS platforms.
• Assist with study validation and low-complexity updates.
• Collaborate with cross-functional teams to ensure timely project setup.
• Maintain documentation and communicate risks and timelines.

Conocimientos

Detail-oriented

Cross-functional collaboration

Communication

Educación

High School Diploma or equivalent

Bachelor's Degree in Life Sciences or related field

Herramientas

CTMS

LIMS

Laboratory databases

Descripción del empleo

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 https://jobs.iqvia.com/benefits.

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.