西安招聘

Work as a Senior Biostatistician-高级统计师

PURPOSE

Develop 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  
•  Indepth 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 

IQVIA（纽交所代码：IQV）是全球专注生命科学领域的高阶分析、技术解决方案和临床研究服务供应商。IQVIA利用深入分析、前沿技术、大数据资源和广泛领域的专业知识，智能连接医疗生态的各个环节。IQVIA Connected Intelligence？快速敏锐地为客户提供强大的数据洞察，帮助客户加速创新医疗的临床开发和商业化进程，以更好的医疗成果惠及患者。IQVIA拥有约72,000名员工，足迹遍布100多个国家/地区。

IQVIA拥有多元化的加强型隐私技术和保障手段，能够在保护个人隐私的同时对信息进行管理和分析，帮助医疗利益相关方有效开展精准疗法，获得更佳的疗效。这些洞见和能力能够帮助生物科技、医疗器械、制药公司、医学研究者、政府机关、支付方以及其他医疗利益相关方，获得对疾病、人类行为和科技进步更深入的理解，共同朝着治愈各类疾病的方向迈进。