Technical Logistics Coordinator

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. Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. Technical Logistics Coordinator/Leader At Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life‑changing medicines to patients. 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.