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Location
Remote (Argentina)
Visa
Sponsors visas in United States, Ireland, United Kingdom; no register of this country names it
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 8, 2026. First seen by Alion on Nov 6, 2026. Parexel scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Parexel is a clinical research organisation headquartered in Durham, North Carolina that provides Phase I to IV clinical trial services, regulatory consulting, market access and safety services to biopharmaceutical companies. Founded in 1983 and owned by EQT and Goldman Sachs since 2021, it employs more than 21,000 people, with large teams in the US, Hyderabad, Bengaluru, London, Poland, Romania, Serbia and Bloemfontein. Its openings are mostly for regulatory affairs consultants and associates, clinical research associates, safety technology analysts, clinical trial managers, data and AI engineers, many of them home or office based.

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.

Technical Logistics Coordinator/Leader

We are seeking a Technical Logistics Coordinator to join our team. As a Technical Logistics Coordinator, you’ll be joining a fast-paced, driven environment that’s helping to make a life-changing difference to patients by supporting the setup, maintenance, and quality oversight of clinical trial logistics systems and data. Through the collaboration and diversity of teams, the Technical Logistics Specialist is provided with multiple opportunities to excel and discover where your skills can take you.

Who we’re looking for

We’re seeking someone who is:

  • Detail-oriented and analytical.
  • Curious and eager to learn technical systems.
  • A strong communicator
  • A proactive problem-solver
  • Reliable and adaptable in a fast-moving environment.

What you’ll do

In this role, you will:

  • Build, maintain, and structure datasets used for clinical trial logistics reporting.
  • Analyze and transform data, including data conversion, merging, filtering, and quality review.
  • Create operational and analytical reports for internal stakeholders.
  • Collaborate with cross-functional CTS&L teams to support logistics planning and execution.
  • Coordinate system setup activities in alignment with project requirements and SOPs.
  • Implement updates and ensure proper documentation within ICH-GxP guidelines.
  • Assess system outputs to ensure accuracy and readiness for project milestones.
  • Manage technical files, logs, and project records.
  • Support continuous improvement of tools, workflows, and data processes.

Additional details

  • Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or related field) required.
  • Experience in a laboratory, scientific, or technical environment preferred.
  • Strong comfort working with digital tools, structured data, and relational database concepts (no programming required, but a “programming mindset” is essential)
  • Ability to work fully home-based in Argentina.
  • Fluency in English required.
  • Familiarity with ICH-GxP or regulated environments is a plus.
  • Experience with Biological Sample Tracking Applications (e.g. Labmatrix) is preferred.

Why join us.

  • Be part of groundbreaking projects that are pushing the boundaries of the industry.
  • Experience a collaborative and inclusive work environment that highly appreciates your expertise.
  • Unlock your full potential with professional growth and development opportunities.
  • Enjoy work-life balance and flexible working hours.
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