bachelor’s degree in life sciences or an equivalent combination of education, training & experience. certified healthcare professional (e.g. registered nurse, licensed practical nurse, md, etc) strongly preferred

生命科学专业或具有相关行业经验，本科以上学历。医疗行业注册人员（例如注册护士，执业护士，医学博士等）优先考虑

excellent oral and written communication skills in english, including proficient presentation skills required

熟练的英文听、说、读、写能力

 excellent communication, collaboration, and problem-solving skills. ability to travel

出色的沟通，协作和解决问题的能力，适应出差

provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.

plan and lead the development of project-related solutions to the full scope of statistical programming tasks.

 programming, testing, and documentation of programs for use in creating statistical ｔａｂｌｅs, figures and listing summaries.

programming of analysis databases (derived datasets) and transfers of data for internal and external clients.

 may perform and plan the programming of database quality control checks.

provide technical expertise to the statistical programming department.

 任职要求： 

 ｍａｓｔｅｒ’s degree life science or computer science with 2+ year relevant experience or bachelor’s degree life science or computer science with 3+ years relevant experience req

 knowledge of statistics, programming and/or clinical drug development process

 working knowledge of computing applications such as base sas, sas/stat and sas macro language

good organizational, interpersonal, leadership and communication skills

applying advanced statistical methods to project work.
ensuring scientific integrity in the application of statistical methodology to clinical trials.
participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.
? perform statistical team lead role on single studies.
? 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.
conduct independent research and teaches courses in statistical methodology.

? bachelor’s degree biostatistics with 7+ years experience req or ｍａｓｔｅｒ’s degree biostatistics with 5+ years experience or ph.d. biostatistics with 2+ years experience
? familiarity with most complex statistical methods that apply to phase i-iv clinical trials.
? in-depth knowledge of applicable clinical research regulatory requirements, i.e., good clinical practice (gcp) and international conference on harmonization (ich) guiｄｅｌines.
? strong working knowledge of sas.
? excellent written and oral communication skills with good interpersonal skills.
? excellent problem solving skills.