Clinical Trial Supply & Project Leader
- Status
- Open
- Remote policy
- Remote
- Employment type
- Not stated
- Salary
- Not stated
- Categories
- Clinical-Supply-Chain, Supply-Chain-Management, Clinical-Operations, Clinical-Research, Project-Management, Clinical-Trial-Management, Clinical-Trial-Supply-Manager, Clinical-Trial-Project-Manager, Clinical-Trials-Project-Manager, Project-Manager-In-Clinical-Trials, Clinical-Research-Project-Manager, Project-Management-(Clinical-Trials), Clinical-Trial-Project-Management, Clinical-Trial-Lead, Clinical-Trial-Supply
- Source
- himalayas
- First observed
- 2026-08-20 07:16 UTC
- Last seen
- 2026-08-20 07:16 UTC
- Source claims posted
- 2026-08-20 06:56 UTC
- Consecutive misses
- 0 of 10
What the posting says
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 experiencedSupply & Logistics Project Manager 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!
Originally posted on Himalayas
Quality
- x Salary range stated weight 35%
- + Remote policy stated weight 20%
- + Location stated weight 15%
- + Organisation stated weight 15%
- + Publication date stated weight 15%
Not enough history yet to judge honesty signals.
Timeline
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#204002 2026-08-20 07:16 UTCPublished