Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Clinical Trial Supply & Project Leader
Job ID R0000038809 Warsaw, Mazovia, PolandAre you ready to lead impactful projects ensuring secure, timely patient treatment in clinical trials?
We're seeking an experiencedClinical Trial Supply & Project Leaderto 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!
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