Overview
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.
Job Description
* 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.
Qualifications
* 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 (written and spoken, mandatory).
* French 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.
Benefits
* 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.
Contact
Quote job ref: JN-032026-6980950
#J-18808-Ljbffr