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Computercraft currently has multiple positions open for Scientific Data Management Specialists. The successful candidates will process, solicit, and provide assistance with data submissions for scientific data from epigenomic and/or genome sequencing...

SummaryThis position is instrumental in ensuring that all statistical programming activities are appropriately planned, organized, and executed for all assigned studies within Clinical Development & Medical Affairs (CDMA) studies.Duties and Responsib...

SummaryThis position coordinates and contributes to the definition, creation, validation, and documentation of CDISC SDTM compliant submission datasets for current and future electronic submissions to regulatory authorities. Duties and Responsibiliti...

SummaryThe senior manager reports to the Director ¿Account Management. The account manager and account management function is responsible for working directly with the business in one or more of the companies business functions: ¿Clinical Devel...

SummaryPrimary responsibilities would be for clinical activities related to the support and commercialization of approved cardiometabolic assets including development, design, and execution of Phase IV studies as well as provision of marketing suppor...

Four to 6 month contract assignmentJob Responsibilities Performs routine analyses of raw materials, drug substances and drug products following established test methods, protocols, and/or planned experiments as written. Maintains laboratory and perf...

SummaryWith oversight from Director, is responsible for the operational management of a large Phase 3 clinical program to evaluate the safety and efficacy of a gastrointestinal drug product. May participate in Medical Affairs and Marketing activities...

SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials Duties and Responsibilities*...

SummaryAssignment of clinical research associate/clinical scientist responsibilities for studies under the direction of the Director or designee, which includes but is not limited to: Preparing protocols and assisting with case report form developmen...

SummaryPerform statistical activities in clinical trials from protocol development to final study report. Provide statistical leadership for the Biostatistics, Statistical programming, and Data Management study team. Provide statistical support to ne...