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Statistician

Responsibilities:

1 Perform a variety of advanced biometrical, statistical, and other technical activities for the design, analysis, and interpretation of statistical data.
2 Develop SAS programs to create statistical tables, listings, and graphics according to the statistical analysis plan.
3 Participate in setting up a study, including developing statistical methodologies, completing the statistical section of a study's protocol, performing sample size estimation, and carrying out randomization procedures.
4 Validate your own programs, perform quality control, and conduct second program validation of other programmers' programs.
5 Participate in CRF design and review and make comments on CRF content.
6 Participate data validation plan meetings.
7 Participate in the blind data review.

Qualifications:

1 Postgraduate degree in biostatistics or a related discipline.
2 At least 1 year of statistical analysis experience in the pharmaceutical field.
3 Excellent communication skills and interpersonal skills.
4 Strong knowledge of ICH-GCP and Chinese GCP.
5 Strong knowledge of and rich experience in SAS programming (5 years of SAS programming experience preferred).
6 Strong spoken and written English communication skills.

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