职位详情

Statistical Programmer

10,000-15,000

北京朝阳区 1-3年 本科
乔治全球健康研究院(澳大利亚)北京代表处

其他单位 其他 20~99人

职位描述
  • 五险一金
  • 节日福利
  • 带薪年假
  • 晋升机会
  • 定期体检
Role Purpose
The Statistical Programmer is responsible for the analysis of medicalresearch projects
conducted in The George Institute, China or from external institute.

Reporting Relationships
The Statistical Programmer will directly report to the Head,Biostatistics and Economic Evaluation Program in Beijing.
Key Accountabilities
 Participate in analysis planning activities in order to meet studyobjectives in compliance
with regulatory requirements.
 Work in collaboration with members of statistics, data management,clinical and project
teams on preparation of study analysis report submitted to studysponsors and regulatory
agencies.
 Participate in the design and implementation of integrated analyses ofmultiple databases.
 Prepare derived datasets for the analyses using SAS software.
 Write programming specifications for analysis files based onstatistical analysis plans.
 Programming using SAS and validate statistical analyses done by junior programmer.
 Work in designing and preparing programs to produce tables andlistings, and figures for
presentation, manuscripts and regulatory submissions based onstatistical analysis plans
 Assist with the development of statistical analysis plans
 Comply with all institute standards and regulatory requirements forthe programming,
analysis and reporting of research projects
 Contribute to write manuscripts that are suitable for publication
 Provide SAS training to members of the statistics teams as required.
 Assist with the preparation of grant applications as required
As a Team Member:
 Participa
Skills, Knowledge and Experience
 Graduate qualifications in Statistics or Epidemiology
 Minimum 3-year experience in statistical programming for medical research
 Experience in multiple aspects of clinical data processing, includingthe analysis of
efficacy and safety data based on the methodology described in thestatistical analysis
plan.
 Understanding of data management principles for clinical trials andmedical research
 Excellent working knowledge of SAS (mandatory) and STATA (desirable) software
 Proficiency in the use of basic and advanced SAS tools and proceduressuch as SAS
BASE, SAS/STAT, SAS/MACRO, PROC REPORT, RPOC TABULATE, ODS, SQL and
additional statistical procedures, and functions.
 Strong focus on quality and timely delivery of work.
 Well organized with good time management skills
 Strong problem solving and analytical skills
 Excellent interpersonal skills with high level of proficiency in English
 Ability to work well and flexibly ie. autonomously, in small teams andwith a wide range of
varying stakeholders
 Ability to see the big picture, whilst still maintaining a focus ondetail and implementation
 Ability to be flexible and adaptable in the face of changingorganisational priorities and
ambiguous environments
 Competence with computer programs (especially MS Office; MS Word, MSExcel, MS
powerpoint) and electronic communication (email and internet).
职位要求
  • 专业要求: 流行病学,药物统计学
  • 最低学历: 本科
  • 工作年限: 1-3年
  • 职称要求: 不限
  • 招聘人数: 1
工作地点
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