For our client, a dynamic international biotechnology company focused on clinical-stage development, we recruit a:Senior/Executive Medical Director - Clinical
Für einen unserer Kunden, ein internationales pharmazeutisches Unternehmen, suchen wir eine/n Clinical Packaging Technician/Operator.Allgemeine Informationen:Startdatum: 01.09.2026Enddatum: 31.12.2026Arbeitsort: Schachen, LuzernHomeoffice: Nein, 100% vor Ort (Onsite)Arbeitspensum: 100%Arbeitszeiten: StandardÜber die Tätigkeit:Die Organisation Global Clinical Supply (GCS) ist für das End-to-End-Management klinischer Studien verantwortlich. GCS überwacht
Position Snapshot Location: Vers-chez-les-Blanc, SwitzerlandEntity: Clinical Research Unit, Nestlé ResearchWork rate: 100%Contract type: Randstad TemporaryDuration: 12 monthsSummaryThe Senior Clinical Trial Assistant (Sr. CTA) provides high-quality operational and administrative support to clinical trial teams throughout all phases of a pharmaceutical study. Operating within a fast-paced, regulated environment, the Sr. CTA ensures clinical documentation
Strategic Business Development & In-Licensing Specialist - 100%Starting date : ASAP Location : GenevaType of role : Permanent role Your ResponsibilitiesGenerate high-level scientific and commercial intelligence on potential licensors and therapeutic target areas.Manage business intelligence tools and databases (e.g., IMS, Evaluate Pharma) to support data-driven decision-making.Actively source, evaluate, and execute prioritized in-licensing
For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking an Associate Specialist within the Downstream Operations group. As a member of the manufacturing team at our client's company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies. General Information: Start date: ASAPDuration: 1 yearExtension: possible (to be
For our client, a leading biotechnology company, we are seeking a Production Planner. General Information: Start date: ASAP/01.09.2026Duration: 12 monthsWorkplace: Luterbach, Solothurn Workload: 100%Working hours: StandardAbout the job: The Production Planner supports manufacturing planning, scheduling, and changeover activities for the Drug Substance (DS) Manufacturing Site, supporting both clinical and commercial programs as well as the CQV phase. In