Senior Biostatistician
摹根麦肯立人才服务（上海）有限公司
- 公司规模：少于50人
- 公司行业：专业服务(咨询、人力资源、财会) 中介服务
职位信息
- 发布日期：2012-11-09
- 工作地点：上海
- 招聘人数：若干
- 工作经验：一年以上
- 学历要求：硕士
- 语言要求：英语熟练
- 职位类别：其他
职位描述
We are looking for Biostatistician or Senior Biostatistician (at least 1 year above experience in clinical research or related area) for leading pharmaceutical companies in Beijing and Shanghai.
Primary Responsibilities:
? Ensures that priorities are consistent with those of Biostatistics
? Provides statistical advice and support to members of Biostatistics
? Deputizes upon request for the Head of the Biostatistics Section
? Assists in ensuring that statistical standards and SOP's are followed within the Section
? Assesses, recommends and develops new standards, policies and procedures
? Programs, validates and documents software in SAS following statistical programming standards and ensures its availability to users.
? Maintains proficiency in in-house computer facilities and associated software
? Interacts with other departments, including Clinical Science, Regulatory Affairs, Project Management, etc., to ensure good coordination and communication
? Provides high quality statistical support to clinical projects.
? Gives input and ensures that drug development strategy, protocols, CRFs and clinical registration documents are in line with ICH and health authority guidelines as well as company internal SOPs and guidelines. Reviews and approves protocols, CRFs and clinical registration documents. Pays special attention to all statistical issues
? Participates in the preparation of drug development plans, especially the clinical development part, and proposes realistic deadlines for statistics tasks.
? Participates, if necessary, in clinical team meetings, project team meetings, study management team meetings and investigator meetings as well as expert meetings and meetings with health authorities
? Leads and manages statistical team if acting as project statistician
? Responsible for the writing of the statistical section of the protocol, stating the hypothesis, defining the planned analysis, primary and secondary variables, time periods, interim analysis specifications, intent-to-treat population and explaining the statistical basis for the choice of sample size.
? Writes statistical analysis plan. Ensures that statistical methods, programming algorithms, data presentations, output deliveries, and timing and load of work are sufficient detailed to execute the analysis smoothly
Requirements:
? Relevant working experience: Minimum 1 year in Biostatistics and Clinical drug development
? Education: MSc (or equivalent) or PhD in Statistics or very similar area.
? Requirements on specific subject(s): Knowledge and experience in the use of statistical software (e.g., SAS) as well as knowledge of databases and interface systems; Communicates clearly and effectively in written reports, data presentations and meetings as required.
? Language: Able to communicate clearly in both written and spoken English.
? Computer skill: Comfortable with Computers; can readily learn new software applications.
? Other skills and/or competence: - Self-motivated and take initiative
Primary Responsibilities:
? Ensures that priorities are consistent with those of Biostatistics
? Provides statistical advice and support to members of Biostatistics
? Deputizes upon request for the Head of the Biostatistics Section
? Assists in ensuring that statistical standards and SOP's are followed within the Section
? Assesses, recommends and develops new standards, policies and procedures
? Programs, validates and documents software in SAS following statistical programming standards and ensures its availability to users.
? Maintains proficiency in in-house computer facilities and associated software
? Interacts with other departments, including Clinical Science, Regulatory Affairs, Project Management, etc., to ensure good coordination and communication
? Provides high quality statistical support to clinical projects.
? Gives input and ensures that drug development strategy, protocols, CRFs and clinical registration documents are in line with ICH and health authority guidelines as well as company internal SOPs and guidelines. Reviews and approves protocols, CRFs and clinical registration documents. Pays special attention to all statistical issues
? Participates in the preparation of drug development plans, especially the clinical development part, and proposes realistic deadlines for statistics tasks.
? Participates, if necessary, in clinical team meetings, project team meetings, study management team meetings and investigator meetings as well as expert meetings and meetings with health authorities
? Leads and manages statistical team if acting as project statistician
? Responsible for the writing of the statistical section of the protocol, stating the hypothesis, defining the planned analysis, primary and secondary variables, time periods, interim analysis specifications, intent-to-treat population and explaining the statistical basis for the choice of sample size.
? Writes statistical analysis plan. Ensures that statistical methods, programming algorithms, data presentations, output deliveries, and timing and load of work are sufficient detailed to execute the analysis smoothly
Requirements:
? Relevant working experience: Minimum 1 year in Biostatistics and Clinical drug development
? Education: MSc (or equivalent) or PhD in Statistics or very similar area.
? Requirements on specific subject(s): Knowledge and experience in the use of statistical software (e.g., SAS) as well as knowledge of databases and interface systems; Communicates clearly and effectively in written reports, data presentations and meetings as required.
? Language: Able to communicate clearly in both written and spoken English.
? Computer skill: Comfortable with Computers; can readily learn new software applications.
? Other skills and/or competence: - Self-motivated and take initiative
公司介绍
摹根麦肯立于1995年成立于英国，为英国各知名金融机构提供高标准的求职者，是众多投资银行和金融服务领域大型企业的首选合作伙。2005年，摹根麦肯立由Imprint Plc公司并购。公司合并后，如虎添翼，业务全面发展，是欧洲发展最快的人才服务公司。2008年，摹根麦肯立公司被Premier Group收购。目前摹根麦肯立在英国、欧洲大陆、中东及亚太地区拥有21个办公室，成为全球人才服务领域的领导者。