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 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 By international regulatory authorities. To lead and manage GCP inspection CAPAs elaboration, approval and followup CQA Audit for CQA manager expected to be also an Auditor as defined in Organisation SOP101134 To work as per the defined strategy for the global clinical audit program (e.g., site, vendor
Später ansehen12.04.24 | Vollzeit | gloor & lang agGloor&lang ist DIE Personalberatung für Life Sciences und der perfekte Partner für High Level Recruiting inund . Wir suchen gezielt Führungskräfte und Spezialisten in den Life Sciences und bieten Lösungen von ad interims Management bis zum on site Contractor. Wir sind Bindeglied zwischen Unternehmen
Später ansehen05.11.19 | Vollzeit | Schlieren | headcount AGApplicable regulations \ Responsible for the coordination of the study team allocated to the project \ Select and manage of CROs, clinical sites, laboratories and other relevant study vendors \ Coordinate and ensure that project activities and trial deliverables are achieved according to timelines, quality
Später ansehen31.10.19 | Vollzeit | Zug | headcount AGManufacturing is a must for this role \ Demonstrated knowledge of cGMP-standard biologics manufacturing & guidelines and product lifecycle management \ Experience with commercial and/or clinical manufacturing in GMP environment \ Knowledge of conjugation or parenteral drug product formulations desirable
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