Project Manager

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

Job summary

Une entreprise mondiale leader dans la chaîne d'approvisionnement des essais cliniques recherche un Chef de Projet pour coordonner la mise en place et la gestion de projets complexes de distribution. Vous serez responsable de la gestion du cycle de vie des projets tout en veillant à la conformité et à l'excellence opérationnelle dans un environnement dynamique et stimulant.

Qualifications

• 2+ ans d'expérience en gestion de projet dans les essais cliniques ou la distribution pharmaceutique.
• Connaissance des réglementations GMP, GDP et des essais cliniques.
• Capacité à gérer plusieurs projets mondiaux simultanément.

Responsibilities

• Être le point de contact principal pour les clients pendant les projets de distribution d'essais cliniques.
• Gérer les délais, budgets et exigences réglementaires des programmes logistiques multicountry.
• Collaborer avec plusieurs services pour offrir des services de premier ordre.

Skills

Gestion des parties prenantes

Communication

Gestion de projet

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.