Global Trade Compliance Pricing Coordinator
- Status
- Open
- Remote policy
- Remote
- Employment type
- Not stated
- Salary
- Not stated
- Categories
- Global-Trade-Compliance, Pricing-Coordinator, Valuation-Specialist, Trade-Compliance-Analyst, Supply-Chain-Compliance, Trade-Compliance-Specialist, Customs-Compliance-Associate
- Tech
- remote-countrylegal
- Source
- himalayas
- First observed
- 2026-09-13 12:26 UTC
- Last seen
- 2026-09-13 12:26 UTC
- Source claims posted
- 2026-09-13 12:21 UTC
- Consecutive misses
- 1 of 10
What the posting says
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.
Global Trade Compliance (GTC) Pricing Coordinator
Position Overview
Parexel is seeking a Global Trade Compliance (GTC) Pricing Coordinator to join our Global Trade Compliance team. This is a newly created role that plays a critical function in ensuring accurate Unit Price governance for clinical trial materials throughout the supply chain.
As the GTC Pricing Coordinator, you will serve as the primary control point for customs unit price validation and approval, ensuring all support documentation related to clinical trial materials unit price, is properly reviewed and assessed in compliance with international trade regulations and sponsor requirements. This role bridges between Sponsor and Parexel Clinical Logistics teams, providing essential oversight that mitigate potential Customs Valuations risks.
About the Role
Key Responsibilities
Unit Price Governance & Compliance
Serve as the primary owner of customs unit price validation activities for sponsor-provided clinical trial materials
Collect, review, and document unit price information from sponsors using approved pricing documentation
Ensure pricing information is accurate, complete, adequately supported, and compliant with company procedures
Review sponsor-provided pricing methodologies and identify potential customs valuation risks
Maintain traceable, audit-ready records supporting all pricing determinations and validation decisions
Support implementation and maintenance of global pricing governance standards
Participate in internal audits, client audits, and regulatory inspections related to customs valuation processes
Monitor changes in customs valuation requirements and recommend process adjustments
Pricing Validation & Quality Control
Perform mandatory unit price quality control reviews before import/export execution
Validate unit prices for medicinal products and sponsor-provided supplies requiring fixed pricing controls
Review supporting documentation for pricing accuracy and completeness
Reject and return pricing records that do not meet validation standards
Approve compliant pricing records and document decisions within designated systems
Serve as the approval gate ensuring no validated material proceeds through import/export without appropriate pricing review
Cross-Functional Collaboration
Partner with Project Management & Delivery (PMD) teams to ensure study materials are properly established within Parexel systems
Collaborate with Sponsors to obtain required unit price information and associated documentation
Support GTC teams by providing validated pricing information for customs invoice preparation
Participate in project meetings to provide updates on pricing validation status
Communicate pricing issues, risks, and delays to stakeholders in a timely manner
Assist with resolution of customs valuation questions raised by customs brokers, government authorities, or project teams
What We're Looking For
Experience & Knowledge
Significant experience in customs valuation, trade compliance, supply chain operations, or pricing governance
Experience with clinical trial supplies, pharmaceutical logistics, or healthcare-related international trade
Strong understanding of customs valuation principles and import/export documentation requirements
Demonstrated expertise in customs valuation methodologies and compliance controls
Proven ability to review and validate data for accuracy and compliance purposes
Experience working within global, cross-functional environments
Strong working knowledge of Microsoft Office applications and database systems
Fluent English communication skills
Skills & Competencies
Strong analytical and problem-solving skills
High attention to detail with ability to identify data discrepancies
Ability to evaluate complex pricing information and supporting documentation
Strong organizational and documentation management skills
Ability to work independently and prioritize multiple activities
Effective verbal and written communication skills
Ability to collaborate effectively across cross-functional global teams
Customer-focused approach when interacting with sponsors and internal stakeholders
Proficiency with Microsoft Office applications, particularly Excel
Ability to work within regulated environments and maintain audit-ready documentation
Strong presentation skills
Education Requirements
Bachelor's Degree in one of the following fields:
International Trade
Supply Chain Management
Logistics
Business Administration
Finance
Economics
Customs & Trade Compliance
About You
You are a subject matter expert in customs valuation and trade compliance who understands the nuances of international trade regulations. You have the ability to identify inconsistencies and potential risks in pricing documentation, and you communicate these findings clearly to both technical and non-technical stakeholders.
You're comfortable working independently while collaborating across multiple departments. You thrive in a regulated environment where attention to detail and documentation are critical. You understand that the work you do directly impacts Parexel's compliance posture and our ability to serve our sponsors effectively.
This role is ideal for someone with a background similar to a Senior GTC Coordinator, with the added dimension of customs valuation expertise. You may come from the pharmaceutical, clinical research, or commercial trade compliance sectors—what matters is your solid foundation in trade compliance and your willingness to apply that expertise to the unique challenges of clinical trial supply chain management.
Location & Work Arrangement
Primary Locations: Argentina or Mexico (Latin America region)
This position is based in Latin America. Candidates from Argentina and Mexico are encouraged to apply. The role requires collaboration with global teams across multiple time zones.
Why Join Parexel?
Parexel is a leading clinical research organization that partners with sponsors to advance healthcare innovation. This newly created role demonstrates our commitment to strengthening our compliance infrastructure and operational excellence. You'll work with a dedicated team in Global Trade Compliance and have the opportunity to shape processes and standards as we scale this critical function.
This is an urgent hire—we're actively implementing pricing governance improvements, and your expertise will be essential to our success. You'll have the opportunity to make an immediate impact on our operations and compliance posture.
Parexel is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees
Originally posted on Himalayas
Quality
- x Salary range stated weight 35%
- + Remote policy stated weight 20%
- + Location stated weight 15%
- + Organisation stated weight 15%
- + Publication date stated weight 15%
Not enough history yet to judge honesty signals.
Timeline
-
*
#728627 2026-09-13 12:26 UTCPublished
-
o
#730409 2026-09-13 14:32 UTCNot seenMiss 1 in a row