Vacatures 121 tot 130 van 169 (ontdubbeld 167)
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Pfizer - Breda
leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope.As a Manager or Senior Manager , your knowledge of the principles and concepts in the- Volledige vacature bekijken
Pfizer - Utrecht
leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope.As a Manager or Senior Manager , your knowledge of the principles and concepts in the- Volledige vacature bekijken
Pfizer - Capelle aan den IJssel
leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope.As a Manager or Senior Manager , your knowledge of the principles and concepts in the- Volledige vacature bekijken
Project Manager - Project Management
Engineering - Amsterdam
Manager is responsible for oversight of assigned clinical studies. The Project Manager will participate in development of Statements of Work (SOW) to define client expectations, and will perform duties associated with day-to-day- Preview - Opslaan
Reverso - Sint Maarten
We have a a Vubis project employee. vacancy for Functieomschrijving Yacht Life Sciences heeft een vacature voor ... Functieomschrijving Yacht Life Sciences has a a Clinical Study Associate. vacancy for Er- Opslaan
Oxfordcorp
study protocols Requirements Life Sciences background Minimum 3 years of pharmacovigilance/ clinical development experience in Belgium Experience with pharmacovigilance systems and safety related product management in60+ dagen geleden - Preview - Opslaan
Icon Plc - Amsterdam
standards and adverse event reporting requirements. Acts as primary site contact and site manager throughout all phases of a clinical research study , taking overall responsibility of allocated sites. Actively develops and- Preview - Opslaan
Derksenderks via Monster Worldwide - Leiden
cycle reviews. You assure the completeness of the Product Specification File and the Study File to facilitate certification of clinical trial materials by the Qualified Person. As QA Manager you participate and contribute to- Opslaan
Nine Zadelhoff Novartis past heel goed bij mij
Novartis
Nine van Zadelhoff werkt al 15 jaar bij Novartis, ze heeft het dan ook erg naar haar zin als clinical study manager (CSM). Ze werkt op de afdeling Trial Monitoring Operations (TMO), die toezicht houdt op de studies van60+ dagen geleden - Preview - Opslaan
Oxfordcorp
of the Client's clinical studies. Exercises independent judgment in planning, organizing, and performing work; monitors performance and reports status to manager . Ensures compliance to the study protocol, domestic and60+ dagen geleden - Preview - Opslaan
Novartis
belang dat we niet alleen naar de vergoeding van één middel kijken, maar het grotere plaatje blijven zien.” Meer weten over wat het werk van Ronald zo waardevol maakt? Nine van Zadelhoff Clinical Study Manager “Ik60+ dagen geleden - Preview - Opslaan
Junior QA Assistant - Project Management
Oxfordcorp - Leiden
required immunological assays. As a QA assistant you will supports one or more project leads in Clinical Immunology with activities relating to coordination of clinical study sample analysis Responsibilities Preparation- Preview - Opslaan
Nvvtg.nl - Utrecht
You will be part of the Clinical Team and report to the Head of Clinical Affairs. Your responsibilities Project management; Clinical study management, including database management, writing and reviewing study - Opslaan