Dear Friends,

We are looking for "Princial Statistician", the following is the JD.　The working place is ：Beijing. Please contact me xju_ql@sina.com if you are interested in this position.
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I.       Job Summary:

A.  Duties and Responsibilities:

¨       Supervision of less-experienced statisticians within project activities¨       Statistical/Biometrics lead for large global or other major programs.¨       Provide statistical input into other disciplines’ activities and participate in interdepartmental processes.

¨       Provision of technical solutions and advice to colleagues and to clients on statistical methodology and principles.

¨       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 Biostatistics’ deliverables within assigned projects.

¨       Develop and coordinate QC procedures for Biometrics deliverables, ensuring activities are appropriate for effectively and efficiently delivering quality output within a specific project.

¨       Statistical analysis of clinical trial data and related decision making.

¨       Responsible for statistical input to statistical reports and Clinical Study Reports.  Authorizes final reports

¨       Provide statistical guidance in development of clinical research program and in design of individual studies as part of multi-disciplinary team; responsible for statistical input to protocol; approves protocol as signatory.

¨       Provide statistical input into design/review of format of CRFs.

¨       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.

¨       Independent peer review of statistical deliverables, eg, protocols, Statistical Analysis Plans, Tables, Figures and Patient Data Listings, statistical reports, Clinical Study Reports.

¨       SAS programming and related activities for the presentation and analysis of clinical trial data.

¨       Contribution to review and amendment of departmental processes and supporting documentation.

¨       Project management activities for identified projects including financial, resource planning and utilization, timelines and milestone management.

¨       Provide support for special committees, eg, DMCs, including input/review of charters, and ensuring maintenance of appropriate blinding.

¨       Contribute to proposal activities and client presentations.

¨       Represent the department during audits.

¨       Carry out all activities according to appropriate  SOPs, working within the framework of the Quality Management System and to GCP.

¨       Perform other duties as requested by management.

B.   Language Skills Required:

¨       Speaking:              Yes        English/Mandarin if located in China

¨       Writing/Reading:   Yes        English/Mandarin if located in China

II.    Education/Qualifications:
Required:

An MSc or PhD in a statistics subject, preferably with a strong medical statistics component.

(Alternative academic qualifications are assessed for comparability.)

III. Experience:
Required:

Approximately 5.5 years’ postgraduate experience in the application of statistics to clinical trials.