職責(zé)描述：
1 Responsible for development of Statistical Analysis Plans, to include statistical methodology, statistical programming procedures, definition of derived variables, data–handling rules and mockups.
2 Responsible for Biostatistics’ deliverables within assigned projects.
3 Develop and coordinate QC procedures for Biometrics deliverables, ensuring activities are appropriate for effectively and efficiently delivering quality output within a specific project.
4 Responsible for statistical input to statistical reports, Clinical Study Reports and publications of the trial.
5 Provide statistical input into design/review of format of CRFs.
6 SAS programming and related activities for the presentation and analysis of clinical trial data.
7 Analysis Datasets and Statistical Output (TLFs) Validation.
8 Review statistical deliverables, eg, protocols, Statistical Analysis Plans, Tables, Figures and Patient Data Listings, Clinical Study Reports.
9 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.
10 provides statistical support to the project team.
11 Performs other duties assigned by manager.
崗位要求：
1 An PhD in a statistics subject, preferably with a strong medical statistics component.
2 At least 2 year of biostatistician experience and working experience in public health and clinical trials is desirable.
3 Considerable skill in SAS programming, being familiar with CDISC data standards is a plus.
4 Knowledge and experience in clinical trials.
5 Fluent in read, written and good oral English.
6 Have good work habits for documenting, standardized coding, and code testing.
7 Have ability for needs’ understanding and analysis, modular thinking, module decomposition, and flow process conduction.
8 Strong communication and coordinate skills, work as a team player.