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 ansehen22.04.24 | Freelancer, Vollzeit, Studentenjobs | Bitterfeld, München, Ulm, Berl | Hays AG - internArchitekt (154) Asset Manager (16) Ausschreibungsspezialist (8) Bauleiter (858) Bauüberwacher (91) Berechnungsingenieur (4) Business Development Manager (4) Claimmanager (6) Disponent (6) Einkäufer (58) Elektroniker (86) Energieoptimierer (6) Facility Manager (122) Geschäftsführer (14) Immobilienverkäufer
Später ansehen16.04.24 | Vollzeit | Basel (Basel-Stadt) | ACHIEVA Group Limited | CHF 69 / Stunde Of the operational trial related documents and procedures, as well as settingup the ESPs and supervising the deliverables of all ESP related activities, from specifications to closeout. For large Phase III or complicated trials, several Clinical Operations Managers might be assigned to a trial for the management
Später ansehen03.04.24 | Vollzeit | Basel (Basel-Stadt) | ACHIEVA Group Limited | CHF 69 - CHF 86 / Stunde Senior Clinical Quality Assurance Manager Work LocationBasel Duration 12 months Contractor Rate CHF 69/hr CHF 86/hr Provide expertise - support for Organisation Clinical Trials To represent CQA for organisations Clinical Trials To work closely with organisation, CRO Clinical Trial Teams
Später ansehen15.04.24 | Vollzeit | Basel (Basel-Stadt) | www.hays.chActivities o Risk management Provide support to the third-party governance and oversight process and ensure Quality Risk Assessments (QRAs) are properly completed and accurate for the different GMA activities (interventional trials, NIS, RWE, RCs and partnerships) o Support External Relations Management
Später ansehen12.04.24 | Vollzeit | Luzern | Universität LuzernNurse (10-20%) Aufgabenbereich - Koordination und Durchführung der Studienvisiten - Selbständige Organisation von Studienaufgaben - Datenerhebung & -management in Studiendatenbank - Durchführung simpler, klinischer Assessments und Tests an biologischem Material Anforderungen - Good-Clinical
Später ansehen29.03.24 | Vollzeit | Luzern | Universität LuzernNurse (10-20%) Aufgabenbereich - Koordination und Durchführung der Studienvisiten - Selbständige Organisation von Studienaufgaben - Datenerhebung & -management in Studiendatenbank - Durchführung simpler, klinischer Assessments und Tests an biologischem Material Anforderungen - Good-Clinical
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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