Research Programmer
Pharma-北京诺华制药有限公司
- 公司规模:500-1000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:2013-07-11
- 工作地点:上海
- 招聘人数:若干
- 工作经验:三年以上
- 学历要求:硕士
- 语言要求:英语良好
- 职位类别:临床数据分析员 临床研究员
职位描述
1. Support programming activities for dry runs, CSRs and publications of individual studies. Responsible for timely, efficient production of assigned programming deliverables (datasets, listings, figures, and tables) with high quality according to defined specifications.
2. With senior guidance and working together with the Biometrician and Statistical Scientist, provide programming support to project-level programming deliverables (for SCS, SCE, RMP), HA interactions and other ad hoc programming requests.
3. Ensure understanding and compliance with study and project programming standards. With senior guidance, provide support to development of programming standards as required.
4. Ensure understanding and comply with defined programming specifications. With senior guidance, provide support to the development of study-level programming specifications as required.
5. Maintain QC compliance and tracking records for the assigned trial/project support.
6. Ensures quality deliverables and compliance with validation process for audit readiness. Provides support to audit preparation as required.
7. Maintain up-to-date, accurate progress of the assigned programming deliverables and ensure high efficiency and timely completion according to agreed timelines.
8. Review eCRFs and edit checks as assigned and assist non-standard data validation programming as needed according to agreed plans for the clinical study.
2. With senior guidance and working together with the Biometrician and Statistical Scientist, provide programming support to project-level programming deliverables (for SCS, SCE, RMP), HA interactions and other ad hoc programming requests.
3. Ensure understanding and compliance with study and project programming standards. With senior guidance, provide support to development of programming standards as required.
4. Ensure understanding and comply with defined programming specifications. With senior guidance, provide support to the development of study-level programming specifications as required.
5. Maintain QC compliance and tracking records for the assigned trial/project support.
6. Ensures quality deliverables and compliance with validation process for audit readiness. Provides support to audit preparation as required.
7. Maintain up-to-date, accurate progress of the assigned programming deliverables and ensure high efficiency and timely completion according to agreed timelines.
8. Review eCRFs and edit checks as assigned and assist non-standard data validation programming as needed according to agreed plans for the clinical study.
公司介绍
北京诺华制药有限公司开发、生产和销售治疗多种疾病的创新处方药,涵盖的疾病领域包括:心血管、内分泌、肿瘤、抗感染、风湿疼痛及骨质疏松、移植免疫、中枢神经以及眼科。北京诺华制药曾获得“***雇主”和“最负社会责任的企业”等殊荣。
“诺华”中文取意“承诺中华”,即承诺通过不断创新的产品和服务致力于提高中国人民的健康水平和生活质量。北京诺华制药成立于1987年,总部设在北京,隶属于瑞士诺华公司。
诺华公司致力于为患者及社会提供创新医药保健解决方案,以满足其日益变化的健康需求。2011年,集团持续经营业务实现净销售586亿美元。集团研发投入约为96亿美元(去除减值及摊销后为92亿美元)。诺华集团总部位于瑞士巴塞尔,业务遍及全球140多个国家和地区,拥有124,000位全职员工。诺华集团立足在中国的长期发展,重要战略投资包括位于上海的综合性生物医学研发中心,以及位于北京昌平的制剂生产工厂和江苏常熟的原料药生产工厂。如需更多信息,敬请登录公司网站http://www.novartis.com和http://www.novartis.com.cn。
“诺华”中文取意“承诺中华”,即承诺通过不断创新的产品和服务致力于提高中国人民的健康水平和生活质量。北京诺华制药成立于1987年,总部设在北京,隶属于瑞士诺华公司。
诺华公司致力于为患者及社会提供创新医药保健解决方案,以满足其日益变化的健康需求。2011年,集团持续经营业务实现净销售586亿美元。集团研发投入约为96亿美元(去除减值及摊销后为92亿美元)。诺华集团总部位于瑞士巴塞尔,业务遍及全球140多个国家和地区,拥有124,000位全职员工。诺华集团立足在中国的长期发展,重要战略投资包括位于上海的综合性生物医学研发中心,以及位于北京昌平的制剂生产工厂和江苏常熟的原料药生产工厂。如需更多信息,敬请登录公司网站http://www.novartis.com和http://www.novartis.com.cn。
联系方式
- Email:staffing.center@novartis.com
- 公司地址:上班地址:建国门外大街1号国贸大厦2座