Senior Statistician
葛兰素史克(天津)有限公司
- 公司规模:150-500人
- 公司性质:外资(欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2013-01-09
- 工作地点:上海-浦东新区
- 招聘人数:1
- 工作经验:五年以上
- 学历要求:硕士
- 语言要求:英语熟练
- 职位类别:临床研究员
职位描述
Reports to: Associate Director Statistics
Job Purpose and Key Responsibilities:
?Taking a lead role in statistical design of protocol, data analysis and result interpretation and regulatory defense
?Managing CROs to ensure compliance with GSK SOPs/standards
?Providing statistical input into drug development strategy in the setting of Therapeutic Matrics Team.
Accountability:
?Operate in collaboration with study personnel to provide input to study protocol, perform sample size calculation, develop randomization schedule, write/review Reporting Analysis Plan, and write/review Statistical Analysis Report and Clinical Study Report
?Assist with or be responsible for communicating study results via regulatory submissions, manuscripts, or oral presentations
?Respond to statistical queries from other functional areas (eg medical, regulatory, and marketing) and to interact with regulators as required.
?Collaborate with data management in the planning and implementation of data quality assurance plans.
?Provide tailored statistics education to less experienced statisticians or other groups if required
?Participate in peer-review of work products from other statistical colleagues.
?Oversee the process and quality of statistical work contracted out to a CRO or research collaborator
?Perform statistical programming if required
Complexity:
?Positive working attitude and excellence in self-motivation
?Strong learning skill and comfortable to adapt to changes
?Ability to negotiate and strategically influence other team members
Specialised Knowledge:
? Knowledge of diseases and drug development process
?Knowledge of statistical theories and application
?Knowledge of clinical trial design elements and potential issues
?Knowledge of statistical application tools and IT technique
Basic Requirements:
?Educated to Ph.D or master degree in Statistics, Math or equivalent field of study
?At least 5 years experience at a multinational pharmaceutical company or international Clinical Research Organization (CRO) as a biostatistician
Preferred Requirements:
?Application of advanced statistical theory and techniques in clinical development
?Self-management skills with a focus on deliverables
?Extra knowledge or experience in Epidemiology, Health Economics or/and Pharmacology is plus
Job Purpose and Key Responsibilities:
?Taking a lead role in statistical design of protocol, data analysis and result interpretation and regulatory defense
?Managing CROs to ensure compliance with GSK SOPs/standards
?Providing statistical input into drug development strategy in the setting of Therapeutic Matrics Team.
Accountability:
?Operate in collaboration with study personnel to provide input to study protocol, perform sample size calculation, develop randomization schedule, write/review Reporting Analysis Plan, and write/review Statistical Analysis Report and Clinical Study Report
?Assist with or be responsible for communicating study results via regulatory submissions, manuscripts, or oral presentations
?Respond to statistical queries from other functional areas (eg medical, regulatory, and marketing) and to interact with regulators as required.
?Collaborate with data management in the planning and implementation of data quality assurance plans.
?Provide tailored statistics education to less experienced statisticians or other groups if required
?Participate in peer-review of work products from other statistical colleagues.
?Oversee the process and quality of statistical work contracted out to a CRO or research collaborator
?Perform statistical programming if required
Complexity:
?Positive working attitude and excellence in self-motivation
?Strong learning skill and comfortable to adapt to changes
?Ability to negotiate and strategically influence other team members
Specialised Knowledge:
? Knowledge of diseases and drug development process
?Knowledge of statistical theories and application
?Knowledge of clinical trial design elements and potential issues
?Knowledge of statistical application tools and IT technique
Basic Requirements:
?Educated to Ph.D or master degree in Statistics, Math or equivalent field of study
?At least 5 years experience at a multinational pharmaceutical company or international Clinical Research Organization (CRO) as a biostatistician
Preferred Requirements:
?Application of advanced statistical theory and techniques in clinical development
?Self-management skills with a focus on deliverables
?Extra knowledge or experience in Epidemiology, Health Economics or/and Pharmacology is plus
公司介绍
葛兰素史克公司在中国的历史最早可追溯至20世纪初叶。自20世纪80年代以来,在中国政府改革开放政策的感召下,公司在中国积极投资,将最先进的制药技术、最优质的产品、最新型的商业模式、***化的管理理念和市场营销技巧引入了中国。
葛兰素威康和史克必成公司于2000年12月完成全球性合并,2002年,葛兰素史克(中国)投资有限公司全面完成业务整合并正式宣布成立,成为中国目前规模***的跨国制药企业之一。公司业务由处方药、非处方药、疫苗和消费保健品4大部分组成,投资公司和地区总部位于北京,主要业务中心分设在上海、天津和香港。
葛兰素史克是最早在中国成功兴建合资企业的外国制药公司之一。在进入中国的20多年间,葛兰素史克先后成立了5家公司,目前2家为合资企业,总注册资本超过2.3亿美元。目前公司在全国28个主要城市(包括香港)设立了办事机构,在全国拥有近3000名员工,为中国的医药行业培养了一大批高素质的商业管理人员和技术骨干。
葛兰素威康和史克必成公司于2000年12月完成全球性合并,2002年,葛兰素史克(中国)投资有限公司全面完成业务整合并正式宣布成立,成为中国目前规模***的跨国制药企业之一。公司业务由处方药、非处方药、疫苗和消费保健品4大部分组成,投资公司和地区总部位于北京,主要业务中心分设在上海、天津和香港。
葛兰素史克是最早在中国成功兴建合资企业的外国制药公司之一。在进入中国的20多年间,葛兰素史克先后成立了5家公司,目前2家为合资企业,总注册资本超过2.3亿美元。目前公司在全国28个主要城市(包括香港)设立了办事机构,在全国拥有近3000名员工,为中国的医药行业培养了一大批高素质的商业管理人员和技术骨干。
联系方式
- 公司地址:天津经济技术开发区第五大街65号 (邮编:300457)
- 电话:13920189515