Project Manager

JR United Kingdom; Peterborough; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading global pharma supply chain company seeks a Project Manager for Clinical Trial Distribution. The role involves coordinating complex distribution projects, ensuring compliance with regulations, and managing client relationships. Ideal candidates will have project management experience in clinical settings and strong communication skills.

Qualifications

• 2+ years’ project management experience within clinical trials or pharma distribution.
• Working knowledge of GMP, GDP, and clinical trial regulations.
• Fluent in English with the ability to manage multiple global projects.

Responsibilities

• Be the primary point of contact for clients across clinical trial distribution projects.
• Manage timelines, budgets, and regulatory requirements.
• Collaborate with Trade Compliance and Logistics.

Skills

Stakeholder Management

Communication

Project Management

Job description

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Project Manager – Clinical Trial Distribution

Global Pharma Supply Chain Company | Fully Remote | UK based

Join a global leader in the clinical trial supply chain, where you'll play a critical role in coordinating the setup, implementation, and maintenance of complex distribution projects for investigational and commercialised products.

What You’ll Do:

• Be the primary point of contact for clients across the life cycle of clinical trial distribution projects.
• Manage timelines, budgets, and regulatory requirements across multi-country logistics programs.
• Collaborate cross-functionally with Trade Compliance, Depot Operations, and Logistics to deliver best-in-class services.
• Lead client meetings, risk assessments, and invoice tracking to ensure operational and financial accuracy.
• Support packaging, labeling, and direct-to-patient services for time- and temperature-sensitive products.

What We’re Looking For:

• 2+ years’ project management experience within clinical trials, pharma distribution, or related logistics.
• Working knowledge of GMP, GDP, and clinical trial regulations.
• Strong stakeholder management and communication skills.
• Fluent in English with the ability to manage multiple global projects simultaneously.

Experience with ePRO or eCOA systems or patient data tools is a plus, but not essential.

Interested in joining a company driving global clinical access and compliance? Apply confidentially today.