Senior Biostatistician - 高级生物统计师招聘_科文斯医药研发（上海）有限公司最新招聘信息-猎才医药网

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职位描述： We are looking for talented clinical research professionals for Senior Biostatistician in Covance Shanghai office. If you have at least 3.5 years of experience in the application of statistics to clinical trials, we want to talk to you about Senior Biostatistician opportunity.Clinical Data, Analysis, and Reporting Organization (CDARO) is providing our clients with unique, reliable and fully integrated service to help them bring the miracles of medicine to market sooner. With CDARO, you have the opportunity to work with some of the biggest names in the pharmaceutical industry. We offer you with a learning environment, comprehensive insight and the road to career success.About the Job:As a Senior Biostatistician, you are responsible for providing statistical services on Phase I-IV clinical trials.Primarily responsibilities of a Senior Biostatistician:? Responsible for development of Statistical Analysis Plans, to include statistical methodology, statistical programming procedures, definition of derived variables, data–handling rules and mockups? Responsible for Statistics’ deliverables within assigned projects? Perform QC of all efficacy and safety datasets and data displays? Statistical analysis of clinical trial data and related decision-making? Responsible for statistical input to statistical reports and Clinical Study Reports. Authorizes final reports as one of Covance signatories? Provide statistical representation on multi-disciplinary team preparing protocol; responsible for statistical input; approves as signatory? Provide statistical input into design/review of format of CRFs? Supervision of less-experienced statisticians within project activities? Prepare randomization specifications; generate schedules; verify randomization components (specification and schedule). Provide input into planning activities related to the preparation of, distribution of and access to randomization and unblinding information? Project management activities for identified projects including financial, resource planning and utilization, timelines and milestone management? Take responsibility for overall status and quality of Statistics’ project documentation, including maintenance of hardcopy and electronic files? Provide statistical input into other disciplines’ activities and participate in interdepartmental processes? Independent peer review of statistical deliverables, e.g., protocols, Statistical Analysis Plans, Tables, Figures and Patient Data Listings, statistical reports, Clinical Study Reports? Provision of technical solutions and advice to Covance staff and to clients on statistical methodology and principles? Provide support for DMCs, ensuring maintenance of appropriate blinding? SAS programming and related activities for the presentation and analysis of clinical trial data? Ensure mechanisms in place to maintain flow of appropriate information between disciplines on project team? Contact with client across multiple disciplinesEducation/QualificationsMSc or higher in a statistics subject, preferably with a strong medical statistics component.Experience? Approx. 3.5+ years of postgraduate experience in the application of statistics to clinical trials? Interpersonal and effective communication skills? SAS proficiency including use of a variety of statistical procedures e.g., non-parametric analysis, linear and non-linear models, categorical data and survival analysis? Experience in the preparation of Statistical Analysis Plans, analysis, reporting, etc? Ability to explain statistical concepts to non-statisticians? An evident appreciation of the possible impact of day-to-day activities and actions on Covance as a business? A professional approach at all timesAbout Covance:Covance is one of the world’s largest and most comprehensive drug development services companies, with more than 11,000 employees in 60 countries. We began operations Asia Pacific in 1988 and today have more than 1000 employees in 14 countries across the region. Through our discovery, nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.Why Covance?At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.We welcome your application and believe this decision may be the most rewarding career move you will ever make! 职能类别：临床数据分析员其他

公司信息

Why Covance? At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We Offer Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. There is no better time to join us!

周边城市招聘：上海浙江安徽广东山东河北重庆北京江苏湖南

企业入驻日期： 2017-11-09

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