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Clinical Trial Supply Specialist

Lausanne Festanstellung CHF100.000 - CHF105.000 p.a. Home Office View Job Description
We are currently supporting an international and innovative healthcare organization in the recruitment of a Clinical Supply Specialist to join its Supply Operations team based in Lausanne. This position plays a key role in ensuring the efficient planning, coordination, and execution of clinical trial supply activities across multiple studies.

hinzugefügt 26/03/2026

  • Innovative healthcare organization
  • Key role in ensuring the efficient coordination of clinical trial activities

Firmenprofil

Internationally recognized healthcare company operating at the intersection of nutrition, pharmaceuticals, and clinical research.
The organization offers a highly collaborative and multicultural environment, with strong exposure to global clinical operations.
It is known for its high standards in quality, innovation, and patient-centric clinical development.

Stellenbeschreibung

  • Coordinate end-to-end clinical supply activities for assigned studies
  • Manage logistics, including packaging, labeling, distribution, inventory, returns, and destruction of clinical materials (IMP / INP / CTM)
  • Develop and monitor supply plans, production forecasts, and inventory strategies
  • Ensure alignment between production schedules, procurement, and delivery timelines
  • Review and contribute to technical documentation (labels, protocols, pharmacy manuals, site instructions)
  • Oversee inventory management within GMP environments and ensure accurate reporting
  • Manage clinical supply activities within IRT systems
  • Collaborate cross-functionally to optimize packaging strategies, distribution models, and blinding approaches
  • Track budgets, purchase orders, and invoices related to clinical supply activities



Anforderungsprofil

  • Proven experience as a Clinical Trial Supply Specialist within a pharmaceutical company or CRO (mandatory)
  • Demonstrated experience coordinating clinical trials across different populations, geographies, age groups, and study types
  • Strong understanding of GMP environments and clinical supply processes
  • Excellent organizational and coordination skills, with the ability to manage multiple priorities
  • Strong stakeholder management and communication skills
  • Fluent English is absolutely mandatory (written and spoken)
  • French is considered a strong asset
  • Degree in Life Sciences, Engineering, Supply Chain, or other scientific related field
  • Minimum 3 years of relevant experience in clinical trial supply specialist

Sonstige Informationen

  • International candidates are welcome to apply
  • The company will support the work permit process in Switzerland for suitable candidates
  • 2-3 days per week of remote working allowed



Referenznummer angeben
JN-032026-6980950

Zusammenfassung

Berufsfeld
Logistik, Einkauf & Supply Chain
Näheres Berufsfeld
Versorgungsplanung
Branche
Healthcare / Pharmaceutical
Ort
Lausanne
Vertragsart
Permanent
Referenznummer
JN-032026-6980950
Art des Jobs
Home Office

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