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)

• 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

• 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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