Project Manager

Verbatim Pharma; United Kingdom; Remote; GBP 40,000 - 80,000; Full time

Job summary

Join a forward-thinking global leader in the clinical trial supply chain as a Project Manager. In this fully remote role, you will coordinate complex distribution projects, ensuring compliance with regulations while managing timelines and budgets. Your expertise in project management will be crucial as you collaborate with cross-functional teams to deliver exceptional services. This position offers the opportunity to work on innovative projects that impact patient care globally. If you're passionate about project management in the pharma industry, this is the perfect opportunity for you.

Qualifications

• 2+ years’ experience in project management within clinical trials or pharma distribution.
• Fluent in English with the ability to manage multiple global projects.

Responsibilities

• Coordinate setup and maintenance of distribution projects for clinical trials.
• Manage timelines, budgets, and regulatory requirements across logistics programs.

Skills

Project Management

Stakeholder Management

Communication Skills

GMP Knowledge

GDP Knowledge

Clinical Trial Regulations

Tools

ePRO Systems

eCOA Systems

Job description

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.

Additional Information:

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Project Management and Information Technology
• Industries: Pharmaceutical Manufacturing and Transportation, Logistics, Supply Chain, and Storage

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