Full TimeAccounting Apply by August 15, 2026

Clinical Laboratory Study Manager

Parexel
Parexel
Buenos Aires·Argentina
Posted on June 14, 2026
Estimated Salary
Not specified
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Description

This is a Full Remote job, available from Argentina.

Our Mission and Values:

When our values align, there's no limit to what we can achieve.

 

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel FSP is looking for a Clinical Laboratory Study Manager. The candidate can be based anywhere in Argentina, Brazil, and/or Mexico.

The Clinical Laboratory Study Manager works closely with Precision Medicine Leadership and cross-functional study teams (i.e. clinical, data management, logistics, laboratory vendor management, etc.) to ensure quality samples and data are proficiently managed to support biomarker and non-biomarker evaluation and enable the delivery of science to medicine for the assigned studies. Will work closely with clinical study management and vendors (central and/or specialty laboratories) to perform project management oversight activities concerning sample tracking, usage, collection, destruction and data processing in alignment with the protocol and regulatory requirements.

Key Accountabilities:

Study Team Support

  • Participates in cross-functional study team meetings and workstreams to support the delivery of the precision medicine strategy for the assigned studies
  • Supports clinical study teams as subject-matter expert for technical and operational matters related to sample management and testing, including anticipating challenges, managing risk and ensuring compliance with regulatory requirements

Requirements

  • Strong knowledge of clinical laboratory operations and regulatory requirements
  • Excellent project management and communication skills
  • Ability to work in a fast-paced environment and prioritize multiple tasks
  • Strong analytical and problem-solving skills
  • Experience working with cross-functional teams and vendors
Interested in this position? Submit your application to Parexel before the deadline.
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DEADLINE: August 15, 2026

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