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高級(jí)SAS統(tǒng)計(jì)編程員（成都）

1.5-2萬(wàn)·13薪
  • 成都武侯區(qū)
  • 3-5年
  • 本科
  • 全職
  • 招5人

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  • 同事很nice
  • 工作環(huán)境好
  • 人際關(guān)系好
  • 團(tuán)隊(duì)執(zhí)行強(qiáng)
  • 交通便利

職位描述

SAS統(tǒng)計(jì)編程醫(yī)藥制造
  • 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
職位福利：五險(xiǎn)一金、績(jī)效獎(jiǎng)金、帶薪年假、補(bǔ)充醫(yī)療保險(xiǎn)、定期體檢、專業(yè)帶隊(duì)、系統(tǒng)培訓(xùn)、帶薪病假

工作地點(diǎn)

成都武侯區(qū)人民南路三段1號(hào)平安財(cái)富中心

職位發(fā)布者

郭女士/HR經(jīng)理

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