Data Management Specialist
上海康德保瑞医学临床研究有限公司
- 公司规模：150-500人
- 公司性质：合资(欧美)
- 公司行业：医疗/护理/卫生
职位信息
- 发布日期：2015-07-04
- 工作地点：北京
- 招聘人数：1
- 工作经验：1年
- 语言要求：英语熟练
- 职位月薪：面议
- 职位类别：临床数据分析员
职位描述
Department: Data Management
Location: Beijing
Reports to: ED of Data Management & Statistical Programming
Principal Accountabilities and Responsibilities:
? Perform all data management activities to ensure the data accuracy and integrity. Support the progress of the project and prioritizes with respect to pre-determined timelines. Work with project teams to ensure smooth transmissions of data.
? The detail data management activities include but not limit to:
? Design Data Management Plan and report the data progress periodically.
? CRF design, review and CRF completion guidelines.
? Data validation Plan development and data validation checks programming.
? SAS programming of listings.
? Generation and tracking of data clarifications form.
? Updating the database and database quality control.
? Blind data review and database lock.
? File archiving for all of the data management documents.
? All other duties as assigned.
Requirements for position:
? College or above education in medical, public health, pharmacology, or other related fields.
? 2 years of industry experience in clinical data management will be preferred.
? Vast knowledge of all stages of data management
? Knowledge of ICH GCP and China GCP
? Familiar with sql and SAS programming is preferred
? Fluent in written and sporken English with CET 6
? Excellent computer and communication skills
? Willingness and capability to take initiative and help Clinical Research and Statisticians resolve data problems
? Be able to work independently and complete a high volume of work
Location: Beijing
Reports to: ED of Data Management & Statistical Programming
Principal Accountabilities and Responsibilities:
? Perform all data management activities to ensure the data accuracy and integrity. Support the progress of the project and prioritizes with respect to pre-determined timelines. Work with project teams to ensure smooth transmissions of data.
? The detail data management activities include but not limit to:
? Design Data Management Plan and report the data progress periodically.
? CRF design, review and CRF completion guidelines.
? Data validation Plan development and data validation checks programming.
? SAS programming of listings.
? Generation and tracking of data clarifications form.
? Updating the database and database quality control.
? Blind data review and database lock.
? File archiving for all of the data management documents.
? All other duties as assigned.
Requirements for position:
? College or above education in medical, public health, pharmacology, or other related fields.
? 2 years of industry experience in clinical data management will be preferred.
? Vast knowledge of all stages of data management
? Knowledge of ICH GCP and China GCP
? Familiar with sql and SAS programming is preferred
? Fluent in written and sporken English with CET 6
? Excellent computer and communication skills
? Willingness and capability to take initiative and help Clinical Research and Statisticians resolve data problems
? Be able to work independently and complete a high volume of work
公司介绍
WuXi PRA Clinical Research (Shanghai) Co., Ltd. offers comprehensive Phase I-IV clinical trial services in Mainland China, Hong Kong and the Asia region. With 5 offices and staff based in 17 cities across China, WuXiPRA’s locally based project teams operate with the support of PRA’s global resources, clinical research expertise, global technologies and SOPs. This centralized operational approach promotes higher quality and outstanding client service. WuXiPRA has invested significantly in staff focused on CFDA regulatory expertise, project management and clinical informatics resources, as well as other support services, including RPS embedded strategic outsourcing.
上海康德保瑞医学临床研究有限公司在中国内地、香港及亚洲地区提供全方位的I-IV期临床试验服务。 康德保瑞在中国有5个办公室，员工分布在17个城市，其团队拥有保瑞医药丰富的全球资源和临床研究专业知识以及全球化的技术和标准操作规程支持。这些有助于全球性、区域性以及本土的临床试验运作达到更高的质量。康德保瑞在人员方面投入巨大，主要集中在CFDA注册专业知识、项目管理、临床信息资源以及包括战略外包服务的其它支持服务方面。
上海康德保瑞医学临床研究有限公司在中国内地、香港及亚洲地区提供全方位的I-IV期临床试验服务。 康德保瑞在中国有5个办公室，员工分布在17个城市，其团队拥有保瑞医药丰富的全球资源和临床研究专业知识以及全球化的技术和标准操作规程支持。这些有助于全球性、区域性以及本土的临床试验运作达到更高的质量。康德保瑞在人员方面投入巨大，主要集中在CFDA注册专业知识、项目管理、临床信息资源以及包括战略外包服务的其它支持服务方面。