长沙招聘

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

    诺思格（北京）医药科技股份有限公司是国内专业领先，规模较大的临床研究合同组织（CRO）之一，总部设在北京，办事处设在上海、长沙、广州、武汉、成都、西安、哈尔滨、南京、沈阳、天津、长春、杭州、合肥等省会城市；在国内覆盖60余个城市，在亚洲覆盖6个国家与地区，已与200余家机构，450余家医院及600多个科室合作，目前已为260多位国内外客户提供国际标准的临床研究外包服务。业务涵盖新药评估与咨询、注册事务、临床试验实施、数据管理和统计分析、医学事务及培训等全方位服务。

“服务医药 服务健康”，详情请登录公司主页： *****************

接收简历邮箱：hr@rg-pharma.com（邮件主题：城市+岗位名称+本人姓名）

【子公司】苏州海科医药技术有限公司为诺思格（北京）医药科技股份有限公司的子公司，子公司成立于2015年01月14日，地址位于苏州工业园区裕新路108号4楼，经营范围包括生物技术开发、生物检测技术服务、会务服务，详情请登录公司主页：*******************************/

【子公司】南京艾科曼信息技术有限公司，专攻于临床研究领域中的数据管理和统计分析环节，全面移植美国CRO的质量标准及管理体系，一步到位与国际CRO行业接轨。同时，服务质量获得欧美主要药厂的认证。自成立以来已完成300余项临床项目，其中部分已经获得美国FDA及欧洲EMEA通过。率先使用国际标准数据管理系统，所有高管均有在美国相关行业从业10年以上经验。总部位于北京，在上海、南京、成都、武汉、合肥等省会设有办公室。