Project Manager

JR United Kingdom; Brighton; Remote; GBP 40,000 - 70,000; Full time

Job summary

A global leader in the clinical trial supply chain is seeking a Project Manager to coordinate the setup and management of distribution projects. This fully remote position offers the chance to work on innovative solutions for clinical trials and commercial products while ensuring compliance and operational excellence.

Qualifications

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

Responsibilities

• Primary contact for clients in clinical trial distribution projects.
• Manage timelines, budgets, and compliance in multi-country logistics.
• Collaborate with various departments for optimal service delivery.

Skills

Project Management

Stakeholder Management

Communication

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.