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!