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

Completeness: 65%

Not enough history yet to judge honesty signals.

Timeline

  1. *
    #204002 2026-08-20 07:16 UTC
    Published