Global Trade Compliance Leader at Parexel

Mexico, chihuahua, Mexico -

Full Time

Start Date

Immediate

Expiry Date

04 Apr, 26

Salary

0.0

Posted On

04 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Trade Compliance, Risk Management, Project Execution, Interpersonal Skills, Leadership Skills, Analytical Abilities, Organizational Skills, Attention to Detail, Self-Motivation, Client Relationship Management, Regulatory Knowledge, Process Improvement, Communication Skills, Teamwork, Problem Solving, Documentation

Industry

Pharmaceutical Manufacturing

Description

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. Develops import/export strategies for projects in collaboration with cross functional teams and in compliance with international trade regulations to achieve project objectives. Prepares actionable plans and ensures all stakeholders are informed and able to execute on established strategies. Serves as a subject matter expert for all trade activities and compliance. Key Accountabilities: Trade Compliance: Evaluate project objectives, products and countries involved and develop import/export strategies for projects that meet local and international trade regulations. Development of import/export strategy: Create and maintain comprehensive project documentation involving all relevant stakeholders and ensuring operational and compliance feasibility. Risk management: Verify the project contracts and ensure tasks and strategies meet contractual obligations with minimum risk to clients and the company. Report and escalate to management as required. Project Execution: 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. Takes responsibility and accessibility for both the strategic planning and the successful execution of all projects/programs/duties as it relates to import/export. Skills: Excellent interpersonal, verbal, and written communication skills and the ability to maintain and develop client relationships. Willingness to work in a matrix environment and to value the importance of teamwork. Excellent leadership skills, and the ability to motivate, influence and collaborate with all levels of management and personnel without direct authority. 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 are ambiguous or incomplete. Highly self-motivated and self-directed. Knowledge and Experience: 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 all regions of the globe, and the ability to understand and work within a multitude of government regulatory schemes and agencies. Solid experience in working with global virtual teams and collaborative environment. Initial experience in risk assessment and process improvement methods to drive continuous improvement. Strong working knowledge of Microsoft Office. Adequate experience in the area of drug development, including supply chain and clinical trials. Demonstrable experience with development of project plans/strategy and actionable deliverables. Initial experience with participating in regulatory and/or client audits. Education: Bachelor’s degree in international business, science, health or related discipline required. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Responsibilities

Develop import/export strategies in compliance with international trade regulations and ensure all stakeholders are informed. Oversee all import/export activities related to projects to ensure compliance with laws and regulations.