本帖最后由 sarahs 于 2016-12-2 16:29 编辑
Statisticians (Shanghai)
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
Statisticians Manager(Shanghai)
Principal Accountabilities and Responsibilities:
• Participate on Medical/Clinical/Regulatory teams supporting clinical studies and projects primarily in the Asian/Pacific region, and work as part of global teams to support global clinical studies and projects.
• Support Data Management in data transfer, data creation, data integrity checks, and data audit.
• Support Statistics in table, listing, and graph generation, and statistical analyses.
• Develop general SAS macros for use by data managers or statisticians.
• Responsible for assisting in recruitment of future colleagues as needed.
• Proficient in SAS Base, STAT, Graph and Macro. Extensive experience using Data _Null_ and Proc Report. Knowledge of SAS SQL or AF/SCL, or Visual Basic is a plus.
• 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
Requirements for position:
• Graduate degree in public health, Biostatistics or related disciplines
• At least 6 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, 4+ years experience of SAS programming would be preferred
• Being fluent in spoken and written English with CET-6.
• Willingness and capability to take initiative and support other clinical research units to resolve variety of statistical related issues
• Mentor or train entry level staff for SAS programming & statistics analysis method
• Provide Statistical training for other departments inside organization and coordinate all the effort with other departments to support organization overall goal
Please contact Sarah Sheng for more details through sarah12087@outlook.com or on +86 21 51001885 |
发表于 2013-7-24 17:53:48