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Clinigen

Project Manager - Clinical Trial Supply (4 months)

Clinigen
Belgium · Full-time · Associate

Do you thrive in fast-paced clinical and pharmaceutical environments?

We're looking for a Project Manager, to lead client projects from planning to execution while ensuring top-quality service and compliance with cGMP standards.

Key Responsibilities

  • Manage clinical supply projects (Phase I-IV) from initiation to completion
  • Act as the primary point of contact for clients, ensuring clear and proactive communication
  • Coordinate internal stakeholders (Operations, QA, Warehouse, Packaging, Distribution) to ensure seamless execution
  • Develop and maintain project timelines, identify risks, and implement mitigation strategies
  • Ensure all project activities are properly documented, tracked, and invoiced
  • Monitor project performance against KPIs (timelines, quality, cost, client satisfaction)

Requirements

  • 5-10 years experience in Project Management within pharma/ clinical trials/ cGMP
  • Strong organizational and coordination skills in multi‑project environments
  • Excellent communication skills and ability to interact with clients and internal stakeholders
  • Proactive, solution‑oriented mindset with strong attention to detail
  • Ability to work under pressure and manage tight timelines
  • Fluent English and French, German is a plus

Benefits

  • Join a collaborative and purpose-driven environment where your work supports improving patient access to essential medicines worldwide
  • Gain valuable hands-on experience within a global life sciences organisation, working alongside knowledgeable and supportive colleagues
  • Benefit from a dynamic and international setting that fosters learning, adaptability, and professional growth
  • Be part of a company that values integrity, teamwork, and a people-first culture
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Posted
May 28, 2026
Type
Full-time
Level
Associate
Location
Mont-Saint-Guibert
Company
Clinigen

Industries

IT Services IT Consulting

Categories

Project Management

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