Key Facts

Remote From:

Hungary , Poland , Czechia , Serbia

Full time

Senior (5-10 years)

English, Czech

Hard Skills

Other Skills

•
Business Acumen
•
Mentorship
•
Creative Problem Solving

Roles & Responsibilities

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

Requirements:

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

Parexel

Pharmaceuticals

About Parexel

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. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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Job description

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