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周边城市招聘： 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期： 2017-11-09
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2年经验 -
招3人 -
英语良好 普通话良好 -
11-09 发布
- 补充医疗保险
- 五险一金
- 交通补贴
- 通讯补贴
- 专业培训
- 年终奖金
- 弹性工作
- 定期体检
职位描述
职位描述： Clinical Data Coordinator*Responsibilities/Duties Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data Generate, resolve and track queries to address problematic data identified during data review activities and apply proper modification / correction to the database Interact with the dictionary coding and maintenance group to ensure appropriate process set-up and application Perform reconciliation of the clinical and safety databases Perform reconciliation of central laboratory and/or third party vendor data (eCRF, eDiary, specialty laboratory, etc.) Perform aggregate review of clinical data by patient, site, and/or project to identify data trends (patient safety, compliance, etc.), and/or data inconsistencies that require further investigation Apply quality control procedures and checks to ensure data quality standards (client and Covance) are achieved Potentially serve as a reviewer of project documents such as protocols, CRFs (or eCRFs and eDiary), monitoring conventions, CRF (eCRF) completion guidelines, etc. Assist with the development of [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consistent, and quality clinical data Assist in the development of the clinical data model and/or database design and annotate the CRF (eCRF) according to these specifications Assist in the creation of data acquisition conventions and data review guidelines / diagnostic specifications consistent with the clinical data model, [statistical] analysis plans, and CRF (eCRF) completion / monitoring conventions Assist in the development and testing of data management system edit / data validation checks (diagnostics) and special listings / procedures used as tools for the data review and discrepancy management activities Potentially interact and collaborate with other project and specialty team members (clinical, programming, statistics, CDM technical support, drug safety, etc.) to support the set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality Potentially serve as client contact for project meetings and CDM status updates Support the training of project staff on project-specific, global, standardized data management processes Perform other duties as assigned by management.*Education/QualificationsBachelor and above*Experience2-3 years 职能类别： 生物工程/生物制药 临床研究员 关键字： CDC Clinical Data Coordinator 生物制药 covance
联系方式
甘井子区大连软件园腾飞园区
公司信息
Why Covance? At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We Offer Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. There is no better time to join us!
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