Clinical Trial Supply & Project Leader

๐Ÿข Parexel ยท all Parexel jobs
๐Ÿ“ Poland
๐Ÿ“… Posted 2026-08-20 ยท via Himalayas
๐Ÿท Clinical-Supply-Chain,Supply-Chain-Management,Clinical-Operations,Clinical-Research,Project-Management,Clinical-Trial-Management,Clinical-Trial-Supply-Manager,Clinical-Trial-Project-Manager,Clinical-Trials-Project-Manager,Project-Manager-In-Clinical-Trials,Clinical-Research-Project-Manager,Project-Management-(Clinical-Trials),Clinical-Trial-Project-Management,Clinical-Trial-Lead,Clinical-Trial-Supply
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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.

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.
๐ŸŒ HIRING LOCATIONS

This role is open to candidates based in: Serbia โ€ข Poland โ€ข Lithuania โ€ข Czech Republic โ€ข 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!

Originally posted on Himalayas

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