Global Trade Compliance 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.

Key Accountabilities:

Trade Compliance

Ensure import/export activities are conducted in compliance with customs and government agencies regulations.
Maintain positive relationship with customs and other government agencies, to learn and gather new requirements and regulations in advance for implement and for issue resolution.
Ensure all documents follow the record keeping process in compliance with Parexel’s and local regulations.
Support with design and implementation of GTC operational and compliance procedures.

(Senior)

Evaluate project objectives, products and countries involved and develop import/export strategies for low to medium complexity projects that meet local and international trade regulations

Project Execution

Provide an efficient interface with customs brokers and ensure import and export clearance are performed efficiently and in compliance.
Prepare and/or submit import and export license application which is aligned with project needs
Attend project meetings to provide import/export updates and support resolution of any import/export issues and possess the ability to determine when to elevate to management for resolution.
Track import/export licenses for quantity and expiry date. Inform and/or prepare and/or submit import/export license application.

(Senior)

Liaise with other departments to establish and maintain effective and relevant import/export activities and support project’s goals.
Oversees all import/export activities related to the project to ensure compliance with laws and regulations in each region.
Continuously inform in advance any import/export restrictions, updates and determine actionable steps which should be taken by the project team.

Skills:

Adequate interpersonal, verbal, and written communication skills and the ability to maintain and develop internal and external relationships.
Willingness to work in a matrix environment and to value the importance of teamwork.
Adequate/Profound leadership skills and the ability to collaborate multi-functional teams.
Fosters and built trust within the company, with the clients and external vendors.
Uses technical and analytical abilities to identify and communicate suggestions for obstacles faced by project teams.
Applies a sense of urgency to resolve problems, performs root-cause analysis and implements viable, permanent solutions.
Solid organizational skills including attention to detail and multi-tasking skills.
Strong attention to detail and ability to resolve situations that is ambiguous or incomplete.
Highly self-motivated and self-directed.

(Senior)

Advanced interpersonal, verbal, and written communication skills and the ability to maintain and develop client relationships.

Knowledge and Experience:

Basic/Adequate knowledge of supply chain, international trade in healthcare or other industry.
Adequate knowledge of customs and/or clinical development.
Adequate experience in communication with customs brokers and other third-party logistic providers.
Basic experience in working with global virtual teams and collaborative environment.
Solid experience in working with global virtual teams and collaborative environment.
Initial/Basic experience in risk assessment and process improvement methods to drive continuous improvement.
Strong working knowledge of Microsoft Office.
Basic/solid experience with development of project plans/strategy and actionable deliverables.
Initial/Basic experience with participating in regulatory and/or client audits.

(Senior)

Possess strong working knowledge of customs and/or clinical trial regulations and ability to apply technical knowledge to complex global business transactions.
Adequate experience with regulatory framework in one or more regions of the globe, and the ability to understand and work within a multitude of government regulatory schemes and agencies.
Initial experience with participating in regulatory and/or client audits.

Education:

Bachelor or Master Degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy, or other health-related discipline, international trade or logistics business

Details

Location

Taipei City, Taiwan

Key Accountabilities:

Trade Compliance

Ensure import/export activities are conducted in compliance with customs and government agencies regulations.
Maintain positive relationship with customs and other government agencies, to learn and gather new requirements and regulations in advance for implement and for issue resolution.
Ensure all documents follow the record keeping process in compliance with Parexel’s and local regulations.
Support with design and implementation of GTC operational and compliance procedures.

(Senior)

Evaluate project objectives, products and countries involved and develop import/export strategies for low to medium complexity projects that meet local and international trade regulations

Project Execution

Provide an efficient interface with customs brokers and ensure import and export clearance are performed efficiently and in compliance.
Prepare and/or submit import and export license application which is aligned with project needs
Attend project meetings to provide import/export updates and support resolution of any import/export issues and possess the ability to determine when to elevate to management for resolution.
Track import/export licenses for quantity and expiry date. Inform and/or prepare and/or submit import/export license application.

(Senior)

Liaise with other departments to establish and maintain effective and relevant import/export activities and support project’s goals.
Oversees all import/export activities related to the project to ensure compliance with laws and regulations in each region.
Continuously inform in advance any import/export restrictions, updates and determine actionable steps which should be taken by the project team.

Skills:

Adequate interpersonal, verbal, and written communication skills and the ability to maintain and develop internal and external relationships.
Willingness to work in a matrix environment and to value the importance of teamwork.
Adequate/Profound leadership skills and the ability to collaborate multi-functional teams.
Fosters and built trust within the company, with the clients and external vendors.
Uses technical and analytical abilities to identify and communicate suggestions for obstacles faced by project teams.
Applies a sense of urgency to resolve problems, performs root-cause analysis and implements viable, permanent solutions.
Solid organizational skills including attention to detail and multi-tasking skills.
Strong attention to detail and ability to resolve situations that is ambiguous or incomplete.
Highly self-motivated and self-directed.

(Senior)

Advanced interpersonal, verbal, and written communication skills and the ability to maintain and develop client relationships.

Knowledge and Experience:

Basic/Adequate knowledge of supply chain, international trade in healthcare or other industry.
Adequate knowledge of customs and/or clinical development.
Adequate experience in communication with customs brokers and other third-party logistic providers.
Basic experience in working with global virtual teams and collaborative environment.
Solid experience in working with global virtual teams and collaborative environment.
Initial/Basic experience in risk assessment and process improvement methods to drive continuous improvement.
Strong working knowledge of Microsoft Office.
Basic/solid experience with development of project plans/strategy and actionable deliverables.
Initial/Basic experience with participating in regulatory and/or client audits.

(Senior)

Possess strong working knowledge of customs and/or clinical trial regulations and ability to apply technical knowledge to complex global business transactions.
Adequate experience with regulatory framework in one or more regions of the globe, and the ability to understand and work within a multitude of government regulatory schemes and agencies.
Initial experience with participating in regulatory and/or client audits.

Education:

Bachelor or Master Degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy, or other health-related discipline, international trade or logistics business