Project Manager

JR United Kingdom; Cambridge; Remote; GBP 45,000 - 65,000; Full time

Job summary

A global leader in the clinical trial supply chain seeks a Project Manager for remote coordination of complex distribution projects. You will ensure timely, compliant delivery of investigational products while managing client interactions and regulatory requirements. Ideal candidates possess 2+ years of project management experience in the pharma or logistics domain, with a strong understanding of industry regulations.

Qualifications

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

Responsibilities

• Primary contact for clinical trial distribution projects.
• Manage timelines, budgets, and regulations across logistics.
• Lead client meetings and ensure operational accuracy.

Skills

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.