sas程序员工作内容

1、负责制定、计划并协调研究项目的编程文档，包括计划和说明； 2、计划并实施：用于生成统计表、图和列表的编程、测试及记录；分析数据集（派生数据集）的编程，及数据的提交；数据库统计核查程序的编写；多个研究/来源数据库中数据合并的编程； 3、基于CDISC标准，编程产生符合递交标准的SDTM、ADaM数据集及其他文档； 4、基于统计分析计划(SAP)，编程生成统计数据图表列表等文件； 5、审核来自内外部的文件，与相关项目人员沟通，提供程序编写支持； 6、负责新技术、SAS宏及应用程序的开发，构建公司相关程序框架体系和程序相关SOP； 7、完成部门的其他相关工作。

岗位职责： 1. 负责按照统计分析计划(SAP),编写SAS程序,生成统计数据图表列表等rtf文件； 2. 负责SAS宏程序的开发，构建公司相关程序框架体系和程序相关SOP； 3. 审核来自统计部的其他同事（统计师、SAS programmer 和DM）的文件，与统计师、数据管理员、QC等相关项目人员沟通，提供程序编写支持； 4. 完成部门的其他相关工作。 任职要求： 1、 本科及以上学历，计算机、统计学、生物统计等相关专业； 2、 1年临床试验领域SAS程序员经验优先； 3、 具备编程技能； 4、 具备英文听说读写能力； 5、 具备良好的团队协作能力。

职责描述： 负责临床试验项目中统计相关工作的具体实施，包括： 1、遵循行业标准，为统计分析提供技术支持； 2、编写程序协助数据经理完成数据清理工作； 3、编写程序制作统计分析数据集； 4、编写程序输出统计分析表格、图表及数据列表的制作。 任职要求： 1.统计学、数学、计算机、流行病与卫生统计学、预防医学等专业本科及以上学历；； 2.英语四级或以上,熟练使用SAS、C、Matlab或R者优先； 3.具有较强团队协作能力、沟通能力和管理能力。 4. 熟悉GCP、CDISC标准者优先。

职位描述: 1、编写SAS程序，制作SDTM/ADaM数据集； 2、 按照统计分析计划，产生统计分析表格、列表及图表； 3、完善、建立和维护各种常用宏； 4、协助数据管理部门进行数据核查。 任职要求： 1、统计学、数学及应用数学、公共卫生、IT、医学、药学相关专业本科及以上学历； 2、熟悉SAS/SPSS/R语言相关统计软件优先，良好的组织、沟通与协作能力； 3、良好的英语/日语听、说、读、写能力优先。

职责描述： 1 Development and documentation of programs used in the production of computer generated outputs for clinical study reports, registration and submission documents, publication requirements plus any other document used to present clinical trials data 2 Communicate with statistician and medical manager to fully understand analysis requirements for assigned clinical projects 3 Perform all SAS programming tasks with high quality in the agreed timeline, and work closely with data management to assure data quality 4 Participate in review of protocol, statistical analysis plan (SAP), data management plan (DMP) and case report form (CRF) 5 Preparation of electronic submission of clinical data 任职要求： 1 BSc, MSc or equivalent experience in information technology, mathematics, statistics or medical documentation 2 In-depth knowledge of Base SAS, SAS/STAT, SAS Graph, SAS SQL and SAS Macro Language. SAS Certification is preferred, not required 3 Knowledge of relevant internal and external standards and guidance for clinical development (CDISC, EMEA/FDA, ICH-GCP etc.) 4 Effective communication skills and ability to establish and maintain effective working relationships with study team members 5 Ability to work under pressure and manage multiple projects simultaneously 6 Solid analytical and problem solving skills paired with strong attention to detail 7 Experience in CDISC, aCRF and XML is preferred 职位福利：五险一金、年底双薪、绩效奖金、通讯补助、补充医疗保险、弹性工作、超长带薪年假

工作职责: 1、撰写分析数据集说明文件，并按此文件编程制作分析数据集，对程序和数据集进行QC 2、根据统计分析计划（SAP）和TFLs模板编写SAS程序，输出TFLs，并完成程序、结果和日志的QC； 3、熟悉相关统计方法，应用SAS软件编程实现描述统计、推断统计和高级统计分析方法； 4、按照CDISC/SDTM/ADaM标准，对数据集进行标准化； 5、外包项目的质控工作 6、其他编程支持工作 任职资格: 1、熟练掌握SAS Bsae、SQL、 SAS STAT； 2、熟悉CDISC标准； 3、工作主动积极、逻辑性思维及较强的分析能力 4、专业要求：数学、计算机、统计学及相关专业 石家庄、南京、武汉、成都、上海

CORE JOB TASK Assistin planning and execution of programming activities for a single project. Assistin the review and input into project requirement including but not limitedin protocol, SAP, CRF, programming specification. DevelopSAS programs for SDTM, ADaM, client-defined analysis dataset, PatientProfiles, Tables, Listings and Graphs of medium-high complexity within asingle project in support of Statistical Analysis Plan, posters,Integrated of Summary of Safety(ISS) and Integrated Summary ofEfficacy(ISE). Supportdata management by generating data listings. Interact with Biostatisticsand Regulatory to design and prepare regulatory submission-ready packages. Actas a Lead programmer for low-medium complex projects. Developproficiency in mock up shell development. RepresentStatistical Programming at internal and client meetings. Actas a Statistical Programming consultant to clients and internal customersin related disciplines e.g. Clinical Data Management, Project Management. Ensurequality of personal work and the work of the team when acting as a LeadProgrammer. Prioritizepersonal workload and that of teammates; Perform work with minimalsupervision. Workon complex problems where analysis of situations or data requires anevaluation of intangible variables; development of technical solutions toabstract problems which require the use of ingenuity and creativity. AdviseSenior Statistical Programming Staff of changes in scope of projects toenable the timely development of change orders. Goodexperience with CDISC standards including Define.xml files. Reviewdraft and final production runs for low-medium complex project to ensurequality and consistency. Carryout all activities according to R&G SOPs working within the frameworkof the Quality management System and to Good Clinical Practice (GCP). Demonstratefull proficiency in technical/programming skills. Contributebroad knowledge of clinical trial activities. Other Accountabilities & Tasks · Assist with interviewing and selection of potential candidates · Provide ongoing training and mentoring within Statistical Programming toensure thorough knowledge of the processes used and ongoing technicaldevelopment. · Perform other duties as requested by management. MINIMUM REQUIREMENTS Bachelor’sdegree and/or equivalent in computer science, statistics, mathematicsor other scientific field (or equivalent theoretical/technical depth). Master degree is preferred. At least 1 year SAS programming experience, preferably in a pharmaceutical/clinical trialenvironment. Fluentin written and spoken English Demonstrateadvance SAS skills good macro programming and SAS/STAT. Independentlyand fully to lead middle complex project

1. 工作职责： a) 根据统计分析计划书编程，负责SDTM和ADaM的产生和QC b) 统计报表和作图制作和QC c) 协助数据管理人员数据清洗 d) 根据相关的SOP/GCP开展工作 2. 岗位要求： 1) 全日制本科或硕士学历； 2) 统计、数学、计算机、医药、生物技术等相关专业； 3) 性格沉稳、热爱SAS软件编程工作或有其他数据分析软件编程经验； 4) 英语读写流利,CET-4或CET-6

CORE JOB TASK Assistin planning and execution of programming activities for a single project. Assistin the review and input into project requirement including but not limitedin protocol, SAP, CRF, programming specification. DevelopSAS programs for SDTM, ADaM, client-defined analysis dataset, PatientProfiles, Tables, Listings and Graphs of medium-high complexity within asingle project in support of Statistical Analysis Plan, posters,Integrated of Summary of Safety(ISS) and Integrated Summary ofEfficacy(ISE). Supportdata management by generating data listings. Interact with Biostatisticsand Regulatory to design and prepare regulatory submission-ready packages. Actas a Lead programmer for low-medium complex projects. Developproficiency in mock up shell development. RepresentStatistical Programming at internal and client meetings. Actas a Statistical Programming consultant to clients and internal customersin related disciplines e.g. Clinical Data Management, Project Management. Ensurequality of personal work and the work of the team when acting as a LeadProgrammer. Prioritizepersonal workload and that of teammates; Perform work with minimalsupervision. Workon complex problems where analysis of situations or data requires anevaluation of intangible variables; development of technical solutions toabstract problems which require the use of ingenuity and creativity. AdviseSenior Statistical Programming Staff of changes in scope of projects toenable the timely development of change orders. Goodexperience with CDISC standards including Define.xml files. Reviewdraft and final production runs for low-medium complex project to ensurequality and consistency. Carryout all activities according to R&G SOPs working within the frameworkof the Quality management System and to Good Clinical Practice (GCP). Demonstratefull proficiency in technical/programming skills. Contributebroad knowledge of clinical trial activities. Other Accountabilities & Tasks · Assist with interviewing and selection of potential candidates · Provide ongoing training and mentoring within Statistical Programming toensure thorough knowledge of the processes used and ongoing technicaldevelopment. · Perform other duties as requested by management. MINIMUM REQUIREMENTS Bachelor’sdegree and/or equivalent in computer science, statistics, mathematicsor other scientific field (or equivalent theoretical/technical depth). Master degree is preferred. At least 3 year SAS programming experience, preferably in a pharmaceutical/clinical trialenvironment. Fluentin written and spoken English Demonstrateadvance SAS skills good macro programming and SAS/STAT. Independentlyand fully to lead middle complex project

岗位要求： 1、生物/医学统计学、数理统计、预防医学等专业； 2、全日制本科以上学历，具有一年以上独立SAS编程完成项目的经验者优先。 岗位职责： 1、审核aCRF, eCRF等相关数据库和数据集结构文件； 2、负责编写和测试数据核查程序； 3、协助数据管理员完成数据库清洗； 4、负责数据管理相关报告的程序编写、维护和运行； 5、编写SAS程序生成SDTM/ADaM； 6、按照统计分析计划编写程序，生成统计图表。 待遇福利： 1.工资构成：月度核定薪资+项目奖金+年终奖金+全勤奖300/月。 2.上班时间:8:30-12:00 13:30-17:30 双休。 3.入职购买五险一金。 4.生日礼金，结婚礼金、生子礼金、节假日礼金、员工体检、年度旅游。 5.可提供住宿。