SAS and Bio statistics recruitment

shiyiming

著名美资企业，热招SAS and Bio statistics，待遇好。有推荐的话请联系annatyco@hotmail.com

1.        Qualification
        Post-Graduate / Ph.D. degree in Statistics
        Over 4 – 8 years of experience as a biostatistician for global clinical trial submissions to regulatory authorities like FDA, EU.

2.        Special Skills and Knowledge
        Clinical Research
        Good Statistical Practice
        Design of clinical trials (concept protocol)
        Sample size estimation
        Randomization
        Statistical programming with tools like SAS
        Handled activities at project/molecule level – development of Statistical analysis plan and other project documents like Master analysis plan

3.        Key Accountabilities
        Development of Statistical sections of protocol
        Calculation of sample size & randomization
        Development of statistical analysis plan, mock tables &
        Develop derived dataset specifications with algorithms and programming notes
        Programming in SAS for analyzing data and producing safety and efficacy tables and listings in specified formats for submission or for other purposes
        Maintain quality and timeliness of assigned project work
        Quality control checks of the generated reports
        Perform any other related activities assigned by the supervisor, such as creation of data files for PK analysis, ESUB activities, mapping, QC of code or generating annual reports
        Assist other staff in programming whenever required