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
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Act as the primary point of contact for clients, ensuring clear and proactive communication
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Coordinate internal stakeholders (Operations, QA, Warehouse, Packaging, Distribution) to ensure seamless execution
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Develop and maintain project timelines, identify risks, and implement mitigation strategies
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Ensure all project activities are properly documented, tracked, and invoiced
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Monitor project performance against KPIs (timelines, quality, cost, client satisfaction)
Requirements
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5-10 years experience in Project Management within pharma/ clinical trials/ cGMP
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Strong organizational and coordination skills in multi‑project environments
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Excellent communication skills and ability to interact with clients and internal stakeholders
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Proactive, solution‑oriented mindset with strong attention to detail
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Ability to work under pressure and manage tight timelines
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Fluent English and French, German is a plus
Benefits
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Join a collaborative and purpose-driven environment where your work supports improving patient access to essential medicines worldwide
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Gain valuable hands-on experience within a global life sciences organisation, working alongside knowledgeable and supportive colleagues
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Benefit from a dynamic and international setting that fosters learning, adaptability, and professional growth
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Be part of a company that values integrity, teamwork, and a people-first culture
