Project Manager

JR United Kingdom; Lincoln; Remote; GBP 50,000 - 70,000; Full time

Job summary

A global leader in the clinical trial supply chain is seeking a Project Manager to manage complex distribution projects. This fully remote position requires strong communication skills and project management experience within the pharma sector. You'll coordinate with cross-functional teams to ensure compliance and operational effectiveness.

Qualifications

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

Responsibilities

• Primary point of contact for clients in clinical trial distribution.
• Manage timelines, budgets, and regulatory requirements.
• Collaborate with various stakeholders to ensure project success.

Skills

Stakeholder management

Communication

Education

Project management experience in clinical trials

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.