| Company Information:
MacroStat (China) Clinical Research Co., Ltd. is a CRO (Contract Research Organization) providing biostatistics and data management services to clinical as well as non-clinical studies in United States (US), Australia, Asia Pacific Region, Japan, United Kingdom (UK), China, and other countries. MacroStat is the unique CRO in China that has been doing projects for submitting to US FDA, CVM (Center for Veterinary Medicine) and EPA (Environment Protection Agency).
Position Title:
Senior Biostatistician / Biostatistician
Duties & Responsibilities:
. Apply statistical theory and methods to the design and analysis for clinical trials in a variety of therapeutic areas. . Prepare data analysis plans and write reports describing results of statistical analysis. . Maintain expertise in new statistical methodologies and applications in pharmaceutical research. . Prepare responses to regulatory agency questions regarding statistical aspects of clinical trials. . Represent the Biostatistics Group in project team meetings and in interaction with regulatory agencies. . Consult with research scientists, medical directors, and clinical managers on statistical questions.
Position Qualifications:
. A degree in biostatistics or statistics, MS or PhD with a strong theoretical background in statistics is required. . Knowledge of SAS programming for statistical analysis and data manipulation is essential. Knowledge of other statistical analysis software is desirable. . The candidate should have 2+ years experience in clinical trials. Experience in supporting global clinical trials is an asset. . Excellent interpersonal skills and ability to communicate effectively. Fluency in English, verbal and written, is essential. . Good project management skills. Ability to engage in clinical, regulatory, scientific programming, and database management groups locally and internationally.
Salary Range:
Benefits:
Web Site:
http://macrostat.com.cn
Application Address:
ailsa.wang@macrostat.com
Contact Email: Ailsa Wang
Application Deadline:
03/03/2012
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