Save Job Back to Search Job Description Summary Similar Jobs Added 26/03/2026Innovative healthcare organizationKey role in ensuring the efficient coordination of clinical trial activitiesAbout Our ClientInternationally 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 DescriptionCoordinate end-to-end clinical supply activities for assigned studiesManage logistics, including packaging, labeling, distribution, inventory, returns, and destruction of clinical materials (IMP / INP / CTM)Develop and monitor supply plans, production forecasts, and inventory strategiesEnsure alignment between production schedules, procurement, and delivery timelinesReview and contribute to technical documentation (labels, protocols, pharmacy manuals, site instructions)Oversee inventory management within GMP environments and ensure accurate reportingManage clinical supply activities within IRT systemsCollaborate cross-functionally to optimize packaging strategies, distribution models, and blinding approachesTrack budgets, purchase orders, and invoices related to clinical supply activitiesThe Successful ApplicantProven 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 typesStrong understanding of GMP environments and clinical supply processesExcellent organizational and coordination skills, with the ability to manage multiple prioritiesStrong stakeholder management and communication skillsFluent English is absolutely mandatory (written and spoken)French is considered a strong assetDegree in Life Sciences, Engineering, Supply Chain, or other scientific related fieldMinimum 3 years of relevant experience in clinical trial supply specialistWhat's on OfferInternational candidates are welcome to applyThe company will support the work permit process in Switzerland for suitable candidates2-3 days per week of remote working allowedQuote job refJN-032026-6980950Job summaryJob FunctionLogistics, Procurement & Supply ChainSpecialisationSupply PlanningIndustryHealthcare / PharmaceuticalLocationLausanne RegionContract TypePermanentJob ReferenceJN-032026-6980950Job NatureHome Office
