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Supply & Logistics Project Manager, Clinical Trials

Summary

Leads clinical-trial supply chains, ensuring compliant, on-time delivery of investigational products and lab samples across multiple countries.

Supply & Logistics Project Manager in Clinical Trials

Location: Warszawa, Masovian, Poland, Czechia, Hungary, Lithuania, Serbia

Employment Type: Local Office

Are you ready to lead impactful projects ensuring secure, timely patient treatment in clinical trials?

We're seeking an experienced Supply & Logistics Project Manager to provide global leadership in clinical and laboratory supply chain management.

You'll combine clinical/lab supply expertise with client understanding to develop optimal solutions, ensuring operational excellence, quality standards, and regulatory compliance.

🌍 HIRING LOCATIONS

This role is open to candidates based in: Serbia • Poland • Lithuania • Czech Republic • Hungary

You must be legally authorized to work in one of these countries.

Key Responsibilities

  • Develop and execute supply strategies for IMP/NIMP, ANS, and laboratory samples
  • Ensure GLP, GDP, GMP compliance across all participating countries
  • Manage project timelines, budgets, and operational resources
  • Oversee third-party providers and negotiate contracts
  • Conduct risk assessments and develop mitigation plans
  • Serve as regulatory point of contact and resolve client issues
  • Lead process improvements and system optimization

Essential Requirements

  • Strong understanding of GxP regulatory framework
  • Extensive pharmaceutical/clinical research/biotech industry experience
  • Proven expertise in laboratory and/or clinical trial supply chain management
  • Excellent project management and operational leadership skills
  • Client-focused approach with strong business acumen
  • Financial management and negotiation abilities
  • Team mentorship and stakeholder management skills
  • Bachelor's degree in biology, pharmacy, health sciences, business administration, or equivalent experience
  • Fluent English (written and spoken)

What Makes You Stand Out

  • Multinational work experience
  • Creative problem-solving in clinical supply chains
  • Proficiency in MS Office Suite

Join our innovative, dynamic international organization and make a significant impact in clinical trial operations. Apply now!

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