Supply & Logistics Project Manager – Clinical Trials

🕒 April 22

🌐 Poland, Hungary, +2 more countries – Remote

🇵🇱 Poland – Remote 🇭🇺 Hungary – Remote 🇱🇹 Lithuania – Remote 🇷🇸 Serbia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

👻 Ghost score 55%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Develop and execute supply strategies for IMP/NIMP, ANS, and laboratory samples • Ensure GLP, GDP, and 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

🎯 Requirements

• Strong understanding of GxP regulatory framework • Extensive pharmaceutical, clinical research, or 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 • Multinational work experience • Creative problem-solving in clinical supply chains • Proficiency in MS Office Suite • Must be legally authorized to work in Serbia, Poland, Lithuania, Czech Republic, or Hungary

🏖️ Benefits

• Join an innovative, dynamic international organization • Opportunity to make a significant impact in clinical trial operations