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Position: Principal Biostatistician, DMC
Institution: Cytel Inc.
Location: Seattle, Washington, United States
Duties: Serves as primary contact for clients and DMCs; Provides guidance and oversight of biostatistics and programming teams in production of statistical analyses and reports, including interim analyses and adaptations, for DMCs; Serves as host for DMC meetings and presents unblinded DMC reports to the DMC in closed meeting sessions; Attends and facilitates project team meetings on a regular basis; Ensures blinding and security of data is maintained, as required by contract, charter, or protocol and in compliance with related SOPs; Adheres to SOPs and applicable regulatory requirements; Develops and facilitates internal and external presentations, as appropriate
Requirements: Master’s or PhD degree in Biostatistics, Statistics, or related field; 3+ years experience (PhD) or 5+ years experience (Master's) working with clinical trial data, ideally in a CRO environment; Expert level knowledge of statistical concepts with working knowledge of medical/scientific terminology; Strong organizational and multi-tasking skills are required, as are excellent verbal and written communication skills; Must read, write and speak English; Prior DMC experience preferred
   
Text: Principal Biostatistician, DMC Serves as primary contact for clients and DMCs; Provides guidance and oversight of biostatistics and programming teams in production of statistical analyses and reports, including interim analyses and adaptations, for DMCs; Serves as host for DMC meetings and presents unblinded DMC reports to the DMC in closed meeting sessions; Attends and facilitates project team meetings on a regular basis; Ensures blinding and security of data is maintained, as required by contract, charter, or protocol and in compliance with related SOPs; Adheres to SOPs and applicable regulatory requirements; Develops and facilitates internal and external presentations, as appropriate Master’s or PhD degree in Biostatistics, Statistics, or related field; 3+ years experience (PhD) or 5+ years experience (Master's) working with clinical trial data, ideally in a CRO environment; Expert level knowledge of statistical concepts with working knowledge of medical/scientific terminology; Strong organizational and multi-tasking skills are required, as are excellent verbal and written communication skills; Must read, write and speak English; Prior DMC experience preferred
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