上海相关职位: 细胞技术员 QC仪器分析检测人员 中药生产车间工艺员 中草药研发工程师 有机合成研究员(II) 有机合成研究员(I) GAC稳定性研究员 产业媒体编辑 CRO 注册专员 Drug Safety Associate
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
职位描述: PURPOSEDevelop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports. Provide training, guidance and mentorship to lower level and new staff.RESPONSIBILITIES? Coordinate the development of analysis plans, table shells, programming and table specifications, the production of tables, listings and figures, data review and statistical analysis.? Perform protocol development, sample size calculation, protocol and CRF review.? Advise data management staff on database design, and critical data. May advise on validation checks.? Write statistical sections of integrated reports.? Provide expert statistical input into and review of statistical deliverables (i.e. analysis plans, table shells, programming and table specifications, data review, tables, listings, figures and statistical sections for integrated reports) and data management deliverables (i.e. database design, validation checks and critical data).? Act as statistical team lead for single complex studies or groups of studies.? Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies. May manage project budget and resource requirements.? Perform the review of RFPs and QIPs, prepare proposal text and attend bid defense meetings.? Manage customer relationships.? Provide training and guidance to lower level and new staff.REQUIRED KNOWLEDGE, SKILLS AND ABILITIES? Excellent written and oral communication skills including grammatical/technical writing skills? Excellent attention and accuracy with details? In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trials? Familiarity with moderately complex statistical methods that apply to applicable clinical trials? Strong individual initiative? Strong organizing skills? Strong working knowledge of SAS computing package? Familiarity with other relevant statistical computing packages such as nQuery? Strong commitment to quality? Ability to effectively manage multiple tasks and projects? Ability to lead and co-ordinate small teams? Ability to solve moderately complex problems? Ability to establish and maintain effective working relationships with coworkers, managers and clients? Working knowledge of relevant Data Standards (such as CDISC/ADaM) 职能类别: 临床数据分析员
枫林路388号枫林国际大厦A座3楼
QuintilesIMS pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster. If that is your passion, we have a place for you.
抗体开发总监-下游 30-80万/年
法规事务高级经理/经理-医疗器械 3-4万/月
医学总监/副总监 3-4万/月
高级医学经理 2-2.5万/月
临床试验医师 (Clinical Trial Physician) 1.5-2万/月
财务助理 4.5-6千/月
EHS专员 5-6千/月
体系工程师 6-9千/月
免疫研究员 1.5-2万/月
验证工程师(职位编号:002) 14-20万/年
安柯瑞原液生产工段长 5.5-7千/月
生物信息工程师 0.8-1万/月
安柯瑞原液生产操作员 4-5千/月
质量工程师 6-9千/月
验证工程师(职位编号:002) 14-20万/年
上海相关职位: 细胞技术员 QC仪器分析检测人员 中药生产车间工艺员 中草药研发工程师 有机合成研究员(II) 有机合成研究员(I) GAC稳定性研究员 产业媒体编辑 CRO 注册专员 Drug Safety Associate
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09