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 Clinical Trial Supply & Project Leader 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.
🌍 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!
Top Skills
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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