Clinical Trial Supply & Project LeaderVerified as a real position

Who we’re looking for

• 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 you’ll do

• 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

About the position

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.

Benefits

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