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Project Manager

JR United Kingdom

Oxford

Remote

GBP 50,000 - 70,000

Full time

7 days ago
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Job summary

Une entreprise mondiale spécialisée dans la chaîne d'approvisionnement des essais cliniques recherche un chef de projet pour gérer la distribution des produits. Vous serez responsable de la supervision des budgets, du respect des délais et de la conformité réglementaire dans un environnement dynamique, collaborant avec des équipes multifonctionnelles pour garantir le succès des projets.

Qualifications

  • 2+ ans d'expérience en gestion de projet dans les essais cliniques ou la distribution pharmaceutique.
  • Connaissance des règlements GMP, GDP et des essais cliniques.
  • Anglais courant, capable de gérer plusieurs projets globaux.

Responsibilities

  • Point de contact principal pour les clients sur les projets de distribution d'essais cliniques.
  • Gérer les délais, budgets et exigences réglementaires.
  • Collaborer avec Compliance, Ops, et Logistique pour des services optimaux.

Skills

Gestion de projet
Gestion des parties prenantes
Communication

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.

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