本帖最后由 sarahs 于 2015-2-9 11:46 编辑
Position: Statisticians
Responsibilities
• Participate in setting up a study including the development of statistical methodology, fill up the statistical section of study protocol, perform sample size estimation, and carry out randomization procedure
• Develop SAS programs to create statistical tables, listings, and graphics according to the statistical analysis plan
• Perform quality control and/or second program validation of other programmers’ programs.
• Participate in CRF design, review , database setup, data validation and ensure that all critical contents are included
• Develop statistical analysis plan, data validation plan, data management plan and blind data review
• All other duties as assigned
Qualifications:
• Graduate degree in public health, Biostatistics or related disciplines
• At least 1 year experience of statistical analysis in a pharmaceutical or CRO setting
• Excellent communication and interpersonal skills
• Knowledge of ICH GCP and China GCP
• Rich experience of SAS programming, 2 years experience of SAS programming would be preferred
• Being fluent in spoken and written English with CET-6.
• Be able to work independently and complete a high volume of work
Pls send CV to sarah12087@outlook.com for more detail. |
发表于 2013-7-25 14:28:47