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NAIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and..
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Job OverviewProvide Trial Master File (TMF) related assistance to study teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory..
Clinical Data Associate III Come discover what our 25,000 employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities..
Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the..
Experience- Min 6 months. Should have experience on all kind of seriousness, causality case reports. Experience on safety narrative writing for fatal serious, non serious cases. Experience in coding of..
Job description Job OverviewManage the process of designing and launching clinical research studies; manage activities of the Sponsor/Clinical Research Organization (CRO); lead colleagues in the design and organization of project..
Responsibilities Develop and review Data Management procedures for clinical trials with sponsor companies and other departments;Establish/negotiate Data Management project timelines and ensure Data Management milestones are met;Coordinate data transfers with..
DescriptionAt ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to..