Project Manager - Clinical Trial Supply (4 months)

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