Project Manager

JR United Kingdom; Kingston upon Hull; Remote; GBP 40,000 - 65,000; Full time

Job summary

A global leader in clinical trial supply chain seeks a Project Manager to coordinate critical distribution projects. You'll manage client interactions and logistics timelines while ensuring compliance with regulations. This fully remote position requires strong project management skills and experience in the clinical trials sector.

Qualifications

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

Responsibilities

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

Skills

Project Management

Stakeholder Management

Communication Skills

Job description

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Project Manager, kingston upon hull, east yorkshire

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Client:

Location:

kingston upon hull, east yorkshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

31.05.2025

Expiry Date:

15.07.2025

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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.

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