Supply and Logistics Specialist
Primary Location: Argentina, Remote Additional Locations: Mexico, Remote 求人ID R0000045239 Category Clinical LogisticsAbout this Role
About Parexel
Parexel is a leading clinical research organization (CRO) committed to advancing patient care through innovative clinical trial solutions. We partner with biopharmaceutical companies to bring life-changing therapies to market faster and more efficiently. Our Supply & Logistics team plays a critical role in ensuring the seamless delivery of clinical trial supplies worldwide, maintaining the highest standards of quality, compliance, and customer satisfaction.
The Opportunity
Are you a supply chain professional with a passion for the biopharmaceutical industry? We're seeking a talented Supply & Logistics Specialist (bilingual) to join our dynamic Clinical Trial Supply & Logistics (CTS&L) team.
In this role, you'll work alongside our Supply & Logistics Project Managers to develop and execute innovative supply chain strategies that keep clinical trials on track, on budget, and compliant with the highest regulatory standards. You'll be the operational backbone of our projects—managing complex logistics, coordinating with global partners, and ensuring our clients receive exceptional service every time.
What You'll Do
Project Management & Strategy
Collaborate with Supply & Logistics Project Managers to develop tailored logistics concepts and solutions that exceed client expectations and drive project profitability
Own study-specific supply chain strategy execution, including sourcing and distribution planning
Maintain visibility of study scope and progress to ensure timelines, budgets, and contractual commitments are met
Proactively identify, manage, and communicate risks and changes to stakeholders
Establish and maintain study-specific management tools and documentation
Optimize resource allocation to ensure appropriate FTE coverage and project requirements are met
Financial Stewardship
Manage Pass-Through Costs (PTC) with rigorous controls and transparent reporting of internal service fees and external provider costs
Operational Excellence
Develop comprehensive clinical supply, sourcing, and distribution strategies in collaboration with cross-functional teams and key stakeholders
Partner with third-party providers to negotiate scope of work and drive value
Plan and manage inventory based on strategy, forecasts, and study requirements
Create and maintain supply schedules, incorporating feedback from clinical teams and adjusting for study progress
Communicate effectively with depot partners to ensure seamless supply chain execution
Who You Are
Experience & Knowledge
Experience in the pharmaceutical, clinical research, or consulting industry
Expertise in clinical logistics or related supply chain functions within the biopharmaceutical sector
Strong understanding of cross-functional activities and how different departments interconnect
Significant multinational work experience
Deep knowledge of GxP regulatory frameworks and ICH GCP guidelines
Fluent in English - oral and written (Mandatory)
Education
Bachelor's degree (B.A./B.S.) or Master's degree in Biology, Pharmacy, International Trade, Business Administration, Logistics, or related health discipline
Equivalent professional experience considered
PharmD or similar advanced qualification valued
Core Competencies
Client-Focused Mindset – You understand that our success is measured by our clients' satisfaction
Strategic Thinker – You can develop creative solutions to complex supply chain challenges
Excellent Communicator – You excel at both written and verbal communication across all levels
Detail-Oriented – You manage multiple tasks with precision and enthusiasm
Collaborative Leader – You thrive in matrix environments and value teamwork
Negotiator – You have proven consultative selling and negotiation skills
Self-Motivated Professional – You take ownership and maintain high standards
Operationally Savvy – You have sound to excellent operational understanding
Tech-Proficient – You're proficient in MS Office Suite and comfortable learning new tools
Why Join Us?
Impact: Directly contribute to bringing life-changing therapies to patients worldwide
Growth: Work on diverse, complex projects that challenge and develop your skills
Culture: Join a collaborative, innovative team that values excellence and continuous improvement
Global Reach: Engage with multinational teams and gain exposure to international clinical trial operations
Compliance & Quality: Work in a highly regulated environment where quality and compliance are paramount
Career Development: Opportunities to mentor, lead, and advance within a growing organization
Parexel is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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