CTMS & LIMS Lab Setup Specialist

IQVIA

Buenos Aires

On-site

ARS 800,000 - 1,200,000

Full time

3 days ago
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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

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.

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