知名TOP外企招聘生物统计师

EricWang

知名外企招聘生物统计师，有外企工作经验的Master或者Fresh PhD都可以看看这个机会。有想致力于生物统计事业的小伙伴也可以看看他们的要求！       

Job Purpose
        The SeniorBiometrician IIis responsible and accountable for leading and delivering statistical analytic solutions relevant to the scientific research objectives formultiple Phase I-IV clinical trials at a trial level by executingRAPs,ensuring high quality and timely production of statistical reporting deliverables (tables, listings and graphs), supporting decision making at the CTT/GCT and working together with other statisticians and the programmer. They support standardization activities which include aligning activities of the individual studies to a MAP and developing computational solutions which lend themselves to easy standardization across multiple programs. They contribute to change initiatives and statistical/analytics research.

Major Activities
1.        Support the statistical team in protocol writing, optimizing clinical trial designs in line with trial objectives, and supporting scenarios simulations and sample size calculations based on relevant technical and disease knowledge.
2.        Responsible and accountable for transcribing MAP aligned RAPs into computational solutions for the statistical programmer to implement(specifications of derived variables, specification and development of statistical computing solutions for inferential statistical analyses, tables and listings templates, and modern statistical graphics for the FIR and CSR) of Phase I-IV clinical trials.
3.        Responsible and accountable for multiple studies RAP execution including the RAP meetings with the necessary CTT members, reporting activities, exploratory analyses/ graphics and additional analyses to support publications for individual clinical trials.
4.        Ensure that documents, specifications, programs/macros are consistent and comply with CSU/project/company standards/processesand provideoperational input into VAPs, specifications of analysis datasets, listings, tables and figures, CSR for Phase I-IV clinical trials ensuring that consistent practices across multiple studies is kept
5.        Ensure to deliver agreed timelines and high qualityfor statistical deliverables and processes, and ensure audit-readiness.
6.        Establish and maintain efficient interfaces with internal and external customers with support of IIS management.
7.        Lead statistical/numerical/analytic research by providing advice and solutions on computational aspects of the problem.
8.        Provide statistical analysis solutions when exploratory analyses are required.
9.        Attend CTT/GCT meetings to help facilitate decision making during design, conduct and reporting of clinical results
10.        Contribute to change initiatives
11.        Contribute to project level activities

我的邮箱是hhwez206@163.com，有想看看这个机会的朋友随时可以和我邮件沟通。