Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
Supply & Logistics Project Manager – Clinical Trials
🕒 April 22
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Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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, 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/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)
🏖️ Benefits
• Health insurance • Paid time off • Flexible work arrangements • Professional development
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