11.04.24 | Vollzeit | Zürich | gloor & lang ag life science careersAnd coordinates internal training programs. On site presence up to 3 days/week tasks- Oversight for QMS Quality Management System- Provides Quality Oversight prior to/ during/ close-out of clinical trials- Leads GCP/GMP/GLP Vendor Qualifications- Organize and lead audits at GCP/GMP vendors
Später ansehen17.03.24 | Vollzeit | Nuremberg | Plexim GmbHA dynamic, owner-managed company with short decision-making processes and a flat hierarchy - A team of passionate scientists and engineers who enjoy sharing their knowledge and view our success as a collaborative effort - A focus on outstanding product quality and long-term customer benefits rather than
Später ansehen17.03.24 | Vollzeit | Cambridge (Middlesex) | Plexim GmbHC2000, STM32, .) - Understanding of power electronic systems and their controls - Strong conceptual thinking and attention to detail during implementation What we offer - A challenging job that requires creative technical solutions - A dynamic, owner-managed company with short decision-making processes
Später ansehen11.11.19 | Vollzeit | Zürich | MT PartnersDesigners, product managers, supply chain experts, customer service and business professionals. Responsibilities Brand Ambassador (Markebotschafter) The Ambassador delivers an unique product experience through one-one engagement with adult smokers, dualist and vapers and therefore this role is fundamental
Später ansehen05.11.19 | Vollzeit | Schlieren | headcount AGTo become a permanent position. The main tasks include mostly organizing projects and leading the project managers, liaising with KOLs, protocol development, CRO selection and management. \ Accountable for the planning, implementation and execution of the clinical trial according to ICH, GCP and other
Später ansehen04.11.19 | Vollzeit | Zürich | Ava AGMore if you don’t hold a PhD Relevant experience in and/or knowledge of at least half of the areas below (by order of importance) - Managing and conducting Phase I-IV clinical trials according to GCP - Managing CROs from the sponsor side - Managing projects in clinical/medical settings - Writing
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