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主题: 500强猎头职位-知名CRO诚聘:SAS programming
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作者 500强猎头职位-知名CRO诚聘:SAS programming   
Morie





头衔: 海归上士

性别: 性别:女
加入时间: 2012/05/29
文章: 10

海归分: 1881





文章标题: 500强猎头职位-知名CRO诚聘:SAS programming (1314 reads)      时间: 2012-6-05 周二, 13:47   

作者:Morie生化制药 发贴, 来自【海归网】 http://www.haiguinet.com

企业介绍:公司是全球医药服务行业的领导者,通过提供创新、优质的专业技术、市场信息和合作方案,适应临床医药、生物科技,医疗卫生事业的需要,提高世界医疗水平。公司为多个医疗领域提供临床研究、中心实验室、数据统计等多项专业服务,服务范围涵盖中枢神经系统、肿瘤治疗、心血管疾病、血栓病、呼吸道疾病、泌尿系统疾病、自体免疫疾病,内分泌疾病和各类感染性疾病等。同时帮助完成了全球最畅销30种药品及最畅销9种生物制剂的研发或者商业化工作,为提高全人类的健康水平做出了贡献。

Responsibilities:
 Performs all SAS programming tasks for a given clinical study or studies, involving investigational or non-investigational drugs, biologics and devices.
 Acts as the primary point of contact for all SAS programming activities for a given clinical study or studies.
 Builds standard tabulation datasets according to certain industry standard or the format requested by client or develops SAS programs to produce data listings and Case Report Form Tabulations as by domain or by subject Displays.
 Builds analysis datasets according to certain industry standard or the format requested by client ba<x>sed on the statistical analysis plan.
 Develops SAS programs to implement statistical analyses as specified in the statistical analysis plans and table shells.
 Performs validation of and quality assurance aspects of all SAS programming activities.
 Represents SAS Programming at project team meetings and provides updates to project team on status of tasks.
 Communicates with Project Biostatistician, Data Manager, Medical Writer, Project Manager and Project Coordinator regarding project issues- Ensures adherence to all timelines associated with SAS programming.
 Ensures integrity of all systems by preserving security and following change control procedures.
 Ensures adherence to guidelines, methodology and SOPs for software development in accordance with FDA, ICH, GCP and SDLC methodology.
 Help junior SAS programmers to grow.
 Other relevant duties assigned for which the incumbent is qualified.

Requirements:
 Bachelor’s degree in biostatistics or related subjects, Master's degree preferred.
 Minimum 3 years SAS programming experience in clinical research line.
 Good skills in the management and resolution of SAS programming issues.
 Demonstrated team-building skills and ability to work successfully in a team environment.
 Knowledgeable in all aspects of the Federal (FDA) regulations and requirements governing the conduct of drug, biologic and device studies including, but not limited to, GCP and ICH requirements.
 Good command of English language and communication skills.

工作地点:大连

作者:Morie生化制药 发贴, 来自【海归网】 http://www.haiguinet.com




标签:  生物统计部,




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