Global Trade Compliance Coordinator

🔥 0 minutes ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Manage import and export operations in Chile and other Latin American countries • Ensure all import/export activities comply with customs and government agency regulations • Build and maintain relationships with customs brokers and government agencies • Monitor regulatory changes • Maintain comprehensive documentation in compliance with Parexel and local regulatory requirements • Design and implement operational and compliance procedures for the Global Trade Compliance function • Serve as the primary interface with customs brokers and logistics providers to ensure efficient clearance • Prepare and submit import/export license applications aligned with project requirements • Attend project meetings to provide updates, resolve issues, and escalate to management when needed • Track and manage import/export licenses, including quantities, expiry dates, and renewal timelines • Support critical clinical research projects and global operations

🎯 Requirements

• Excellent interpersonal, verbal, and written communication skills • Ability to build strong relationships • Proven ability to thrive in matrix environments and collaborate effectively across functional teams • Strong analytical and problem-solving abilities • Sense of urgency in resolving issues • Exceptional organizational skills with meticulous attention to detail and strong multitasking abilities • Self-motivated and self-directed • Ability to work independently in a remote environment • Solid knowledge of international trade in Clinical Trials or healthcare industries • Adequate knowledge of customs regulations and clinical development processes • Demonstrated experience communicating with customs brokers and third-party logistics providers • Solid experience working with global virtual teams in collaborative environments • Strong proficiency with Microsoft Office Suite • Experience with risk assessment and process improvement methodologies • Fluent English • Bachelor's or Master's degree in biology, pharmacy, health-related discipline, international trade, or logistics

🏖️ Benefits

• Flexible remote work arrangements • Supportive company culture • Opportunity to develop expertise in international trade compliance within the clinical research industry • Opportunity to work with a talented, collaborative team across Latin America and beyond • Opportunity to support meaningful clinical research that impacts global healthcare