8 Clinical Trials Data Manager Jobs
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Senior Clinical Data Scientist Ireland , Transfer and conform of Clinical trial data to NCDS compliant standards. The position is a key contributor with Data Provisioning team in ensuring that pharmaceutical drug-development plans in Novartis 2 days ago
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Clinical Operations Program Associate Director Dublin, County Dublin, Ireland cycle time, patient enrollment), based on the clinical intelligence package received from the Health Insights Manager and other data sources - Defines an optimal geographic country footprint and proposed 7 days ago
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Principal Clinical Data Science Lead ICON Clinical Research Ltd - Dublin for managing data management teams, studies, and programs of studies under the general direction of the Senior Manager/Director of Data Management. The Principal Clinical Data Science Lead will provide planning 12000.0 12 days ago
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Medical Device Director Ireland Supplier Quality Engineer Galway LIMS Templator / LIMS Data Entry Dublin Senior Regulatory Affairs Specialist Dublin Principal Research Engineer Galway R&D Senior Program Manager Galway C&Q Engineer Dublin 8 days ago
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Technical Transfer Engineer - Drug Substance Leinster, Ireland Carlow Mechanical Project Engineer Limerick Quality Compliance Lead Donegal Associate Director Clinical Trial Capabi Cork Clean Utilities Engineer Carlow Master Data Specialist Dublin Cleaning Validation More than 30 days ago
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Medical Study Manager Life Science Recruitment Ltd - Cork Manager you will ensure the safety and wellbeing of the Participants on the clinical trial. The Medical Study Manager be responsible for completing specialised health related assessments and reviewing 100000.0 26 days ago
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Staff R&D Engineer- Customer Focus Dublin, County Dublin, Ireland Project Engineer Cork Associate Director Clinical Trial Capabi Cork Manufacturing Engineer Limerick Process Engineer Limerick Lead Maintenance Reliability Engineer Westmeath Senior QA/RA Specialist Galway More than 30 days ago
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Medical Research Study Manager CPL Healthcare - Cork the safety and wellbeing of the Participants on the clinical trial, and to complete specialized health related assessments and reviewing of safety data in accordance with ICH-GCP principles. They will need €70000 to €80000 Per year More than 30 days ago
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