Project Manager

JR United Kingdom; Chesterfield; Remote; GBP 35,000 - 55,000; Full time

Job summary

A global leader in clinical trial supply chain seeks a Project Manager to coordinate distribution projects. This remote role involves managing client interactions, timelines, and regulatory compliance while collaborating across teams to ensure project success. Ideal candidates will have project management experience in the pharma sector and strong communication skills.

Qualifications

• 2+ years’ project management experience in clinical trials or pharma distribution.
• Fluent in English and able to manage multiple global projects.

Responsibilities

• Lead and manage clinical trial distribution projects.
• Collaborate with various teams to ensure compliance and efficiency.
• Support packaging and direct-to-patient services.

Skills

Project Management

Stakeholder Management

Communication

Knowledge of GMP and GDP

Job description

Social network you want to login/join with:

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.