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Supply and Logistics Specialist

Parexel

🇬🇧 English
GxP regulatory frameworks ICH GCP guidelines

Descripcion del puesto

About the role

Parexel is seeking a Supply and Logistics Specialist to join its Clinical Trial Supply & Logistics (CTS&L) team. The role supports project managers in designing and executing supply chain strategies that keep clinical trials on schedule, within budget, and fully compliant with regulatory standards.

Key responsibilities

  • Collaborate with Supply & Logistics Project Managers to create tailored logistics concepts and drive project profitability.
  • Own study‑specific supply chain strategy execution, including sourcing, distribution planning, and inventory management.
  • Maintain visibility of study scope, timelines, budgets, and contractual commitments.
  • Identify, manage, and communicate risks and changes to stakeholders.
  • Develop and maintain study‑specific management tools, documentation, and supply schedules.
  • Manage Pass‑Through Costs with rigorous controls and transparent reporting.
  • Partner with third‑party providers to negotiate scope of work and deliver value.

Required profile

  • Experience in the pharmaceutical, clinical research, or consulting industry.
  • Expertise in clinical logistics or related supply chain functions within the biopharmaceutical sector.
  • Significant multinational work experience.
  • Deep knowledge of GxP regulatory frameworks and ICH GCP guidelines.
  • Fluent English communication skills.
  • Bachelor’s or Master’s degree in Biology, Pharmacy, International Trade, Business Administration, or related field.

Required skills

  • GxP regulatory frameworks
  • ICH GCP guidelines

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