Project Manager - Clinical Trial Supply (4 months)

About the role

We are seeking an experienced Project Manager to lead clinical supply projects across all trial phases (I‑IV). You will act as the main liaison for clients, ensuring seamless coordination between internal teams and delivering projects that meet cGMP standards.

Key responsibilities

• Manage end‑to‑end clinical supply projects from initiation through completion.
• Serve as the primary point of contact for clients, providing proactive communication.
• Coordinate internal stakeholders—including Operations, QA, Warehouse, Packaging, and Distribution—to guarantee smooth execution.
• Develop and maintain detailed project timelines, identify risks, and implement mitigation strategies.
• Ensure all project activities are documented, tracked, and invoiced accurately.
• Monitor performance against KPIs such as timelines, quality, cost, and client satisfaction.

Required profile

• 5‑10 years of project management experience in pharma, clinical trials, or cGMP environments.
• Strong organizational and coordination abilities in multi‑project settings.
• Excellent communication skills for interacting with clients and internal teams.
• Proactive, solution‑oriented mindset with meticulous attention to detail.
• Ability to work under pressure and meet tight deadlines.
• Fluent in English and French; German is a plus.

Required skills

What we offer

• A collaborative, purpose‑driven environment focused on improving patient access to medicines.
• Hands‑on experience within a global life‑sciences organization.
• Opportunities for learning, adaptability, and professional growth in an international setting.
• A culture that values integrity, teamwork, and a people‑first approach.