Trial Supplies Manager

JR United Kingdom; Uxbridge; Remote; GBP 50,000 - 80,000; Full time

Job summary

A leading global biopharma company is seeking a Global Clinical Supply Manager in Uxbridge. The role involves designing supply strategies for clinical trials, collaborating with various teams, and ensuring compliance with regulatory frameworks. Join an innovative organization committed to improving patient outcomes through precision medicine.

Qualifications

• Clinical supply chain experience in a global pharmaceutical or biotech environment.
• Strong knowledge of regulatory frameworks.
• Proficiency in IRT/IVRS systems and clinical study planning tools.

Responsibilities

• Design and manage supply strategies for investigational products.
• Collaborate with cross-functional teams on delivery plans.
• Anticipate and address risks in inventory and distribution.

Skills

Clinical supply chain experience

Strong knowledge of drug development lifecycle

Proficiency in clinical forecasting

Exceptional communication

Project management skills

Job description

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Trial Supplies Manager, london (uxbridge)

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Client:

Planet Pharma

Location:

london (uxbridge), United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

10.06.2025

Expiry Date:

25.07.2025

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Job Description:

? Global Clinical Supply Manager – Innovative Biopharma

? Location: Remote with office visits twice a month

? Duration: Full-time - 6 month contract to start with

? Function: Clinical Supply Chain, Clinical Operations, Global Development

Are you ready to help shape the future of clinical development and play a key role in delivering life-changing medicines to patients around the world?

A leading global biopharma company with a robust pipeline in oncology, haematology, immunology, and cardiovascular disease is seeking an experienced Global Clinical Supply Manager to join their expanding Global Clinical Supply Chain (CSC) organization. This team sits at the heart of a dynamic and integrated supply chain built to support the growing demand for personalized and targeted therapies.

What You’ll Do:

As a Global Clinical Supply Manager, you will:

• Design and manage supply strategies for investigational products across all phases of clinical development.
• Collaborate with cross-functional teams—Clinical Development, Regulatory, Manufacturing, Quality, and external vendors—to align on forecasting, labeling, packaging, and delivery plans.
• Anticipate and address risks, proactively managing inventory, use-dates, and distribution strategies.
• Influence key study design decisions and contribute to clinical protocol planning.
• Serve as the primary supply point of contact for assigned studies and compounds.
• Support inspection readiness and quality compliance efforts.
• Leverage IRT systems to manage site-level supply strategies and randomization approaches.
• Provide input on budgets and procurement planning, including oversight of commercial comparator sourcing.

What You Bring:

Clinical supply chain experience in a global pharmaceutical or biotech environment

Strong knowledge of the drug development lifecycle and regulatory frameworks

Proficiency in clinical forecasting, IRT/IVRS systems, and clinical study planning tools

Proven ability to collaborate across departments and vendors

A strategic mindset with a passion for solving complex logistics challenges

Exceptional communication, project management, and influencing skills

Why Join Us?

You'll be part of a mission-driven organization that is redefining how investigational medicines reach patients—faster and more efficiently. This is a unique opportunity to work within an innovative, future-focused model where clinical and commercial supply chains converge, enabling better outcomes through precision medicine.

If you're ready to make an impact and grow your career in a purpose-driven, collaborative environment, let’s connect.