31.05.24 | Vollzeit | Zürich | jobwinner.chHematopoietic stem cell product for a phase I/II clinical trial. Technical Project Manager CMC & ATMP - Pharmaceutical Environment Your responsibilities - Responsibility and accountability for the chemistry, manufacturing, and controls (CMC) development of a gene therapy medicinal product (GTMP). - Design
Später ansehen30.05.24 | Teilzeit | Solothurn | Ypsomed AGPassion. Ypsomade. In the area of Quality Management, Regulatory and Medical Affairs in Solothurn, we are looking for an experienced and passionate person to join the Medical Affairs team as a Clinical Research & Evaluation Manager 80% Ref. No. 6953 Location Solothurn Hybrid Help us bring
Später ansehen29.05.24 | Vollzeit | Baden | gloor & lang ag life science careersCoordination of internal trainings, manage related projects andsupport cross-fct teams. On site presence up to 4 days/week tasks- Oversight for QMS Quality Management SystemProvides Quality Oversight prior to/ during/ close-out of clinical trialsLeads GCP/GMP/GLP Vendor QualificationsOrganize
Später ansehen29.05.24 | Vollzeit | Baden | gloor & lang ag life science careersCoordination of internal trainings, manage related projects andsupport cross-fct teams. On site presence up to 4 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
Später ansehen06.05.24 | Vollzeit | Hays AGCompliance with recognized medical/ ethical standards related to the marketing of PHCI products o Defending challenges from authorities and competition o Manages and collaborates Key Opinion Leaders to drive brand advocacy and build scientific credibility o Managing/ enabling P&G and third-party HCP
Später ansehen06.05.24 | Vollzeit | Hays AGFSC Manager (m/f/d) Freelance/temporary employment for a project Basel Stadt Start date asap Reference number 760418/1 Partager ou imprimer ce job Your responsibilities o 3rd Party Contracts - PO Management (PHAG and NPC) o Clinical Trial Refund Process o IFRS 16- Lease SPOC o Month End Reporting
Später ansehen06.11.19 | Vollzeit | Zug | headcount AGDocuments, illustrations and video. Examples include presentations, educational materials, event briefings and scientific publications. You will ensure all work is of the highest standard with close attention to detail. Project management is an integral part of this role, whether for coordinating parallel
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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