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Posted:

Biostatistician_010m

Company
- A world famous medical industry

Location
- Beijing

Overall Responsibility

Overall responsibility for designing, planning, SAS programming,
analysing and reporting the statistics in the given clinical studies.

Responsibility

- Give statistical input to protocol with regards to design, sample size,
choice of and analysis of endpoints.
- Review protocol, Case Record Form and Trial Validation Plan.
- Prepare Statistical Analysis Plan (SAP) including table shells.
- Prepare for and participate in database release meeting.
- Develop SAS programming, conduct statistical analyses
and ensure preparation of output according to SAP.
* Conduct additional analyses for publications of the trial.
- Review of Clinical Trial Report, presentation slides and scientific
publications for statistical and scientific contents.
- Ensure documentation for the trial in accordance to ICH E9, GCP and SOPs.
- Ensure adherence to all timelines associated with biostatistical activities.

Requirement

- Bachelor degree in scientific or biomedical area, preferable major
in statistics, master degree is desirable.
- 2 years of biostatistician or SAS programming experience,
working experience in clinical studies is desirable.
- Knowledge and experience in designing and planning clinical trials.
- High degree of skill in the resolution of SAS programming issues
and sample size calculation softwares.
- Fluent in written and spoken English.
- Ability to plan and prioritise complex tasks
and approach these in a flexible manner.
- Ability to work effectively as a good team member.

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