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简历投递： yujie.ma@excel-cro.com
职位性质： 兼职/实习 有效日期： 2010年04月06日 至 2010年05月06日
招聘人数： 2 人
工作地点： 上海
职位描述： Jr.Biostatistician
Responsibilities
 Assists in study design and development of statistical section in clinical trial protocols
 Assists sample size and statistical power calculations and randomization schedule generation
 Attributes to development of statistical analysis plans including table shells design for individual studies
 Supports data safety monitoring board (DSMB) or data monitoring committee (DMC) and clinical endpoints committee (CEC) regarding to statistics analysis
 Participate in statistical support for CRF design, database development, data validation plan and blinded data review
 Performs SAS programming to generate tables, listings, figures, and statistical analyses
 Assists higher level biostatisticians for the project tasks
 Conducts literature searches to support statistical team
 Performs other duties assigned by supervisor
Qualifications
 An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field
 Experience of statistical analysis in the pharmaceutical industry is preferred
 Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
 Be knowledgeable in drug agencies (e.g. FDA) regulations and requirements governing the conduct of drug and medical device studies including, but not limited to, GCP and ICH requirements
 Good communication and interpersonal skills
 Proficient working in a PC/Windows environment
A good command of English language if one’s native language is not English
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发表于 2010-4-30 20:25:23
发表于 2010-5-1 21:00:36