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statistics, biostatistics, or related field required. PhD preferred. 15+ years of experience in drug development 5-10 years of experience in vaccine development At least 5 years of managerial experience in
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throughout clinical drug development in collaboration with pharmacometrics and statistics (as relevant). Provides recommendations for clinical doses and dosing algorithms (including drug interaction advice
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-functional teams to provide effective statistical consultation with scientists and toxicologists. You will collaborate with scientific colleagues across a diverse set of disciplines in DSRD, on the design
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of experience OR Masters Degree with 6+ years of experience OR PhD with 2+ years of experience • Degree preferably in engineering, economics, statistics, computer science, or related quantitative field
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on deliverables throughout the process Provide input for the design of the Statistical Analysis Plan (SAP) and the clinical data output Responsible for review of patient level data across a study and for
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information into clear, concise, and well-structured documents that can be easily understood and followed by researchers, clinicians, and other stakeholders involved in the studies. Qualifications MD or PhD
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across various fields, our team leverages advanced statistical analysis, machine learning techniques, and data visualization tools to uncover patterns, trends, and correlations within the data
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set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
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degree, preferably in a life science discipline. BS/BA +5 years, MS/MA +3 years, PhD +0 year s of experience in medical writing or related field. Understanding of the role of each member of cross
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, Excel, Word, Outlook and PowerPoint. Excellent interpersonal and organizational skills . Nice-to-Have Master's degree (MA/MS/MBA) and 7+ years of experience . Doctorate (PhD/PharmD/JD) and 4