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精鼎医药研究开发(上海)有限公司
宣讲会时间:2015年10月28日18:30~20:30
宣讲会地点:沈阳药科大学新科研楼五号教室(图书馆1楼)
公司名称:精鼎医药研究开发(上海)有限公司2016年校园招聘专场宣讲会
招聘职位:1.Statistical Programmer I ( 统计编程师 )
2.Clinical Data Analyst ( 临床数据分析员 )
3.Drug Safety Associate ( 药物安全助理 )
申请以下校园招聘职位,请将简历发送至:tony.feng@
统计编程师 Statistical Programmer
Key Accountabilities:
The Statistical Programmer works closely with Data Operation groups to support various programming activities related to the statistical analysis and reporting of clinical study data.
Ensure compliance with WSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations and participate in internal/external audits and regulatory inspections as required, Use efficient programming techniques to produce high quality derived datasets, tables, figures and data listings.
Education and Skills:
l Educated to BS or above degree level in the relevant discipline is preferred or equivalent work experience. (Statistics, Pharmacy, Mathematics, Applied Mathematics, Computer Science, Biological science, or other health-related discipline preferred)
l Experience in SAS
l Good in written and oral English
l Demonstrate ability to learn new systems and function in an evolving technical environment
l Attention to detail
临床数据分析员Clinical Data Analyst
Key Accountabilities:
The role of the Clinical Data Analyst is to perform assigned tasks or activities in clinical data management. All tasks should be performed in accordance to corporate quality standards or international regulatory requirements.
Activities may include Development of database build specifications, User Acceptance Testing (UAT), data validation and cleaning, generation and integration of queries, running of reports with high levels of direction/supervision, Data reconciliation tasks, Identifying and reporting protocol deviations. Support site monitoring personnel to retrieve missing data as required. Provide work status updates regularly to direct supervisor. Other assigned responsibilities as needed.
Education and Skills:
l Good interpersonal, verbal and written communication skills
l Knowledge of medical terminology
l Ability to work in team environment
l Good analytical skills and attention to detail
l Effective time management to meet daily metrics or team objectives
l Bachelor’s degree and / or other medical qualification or relevant DM experience
药物安全助理Drug Safety Associate
Key Accountabilities:
Performing clear and accurate data capture of Individual Case Safety Reports (ICSRs) (including serious and non-serious cases from spontaneous and clinical trials origin, literature and E2B cases; and veterinary cases, as applicable) and appropriate medical assessment (including company causality and assessment of expectedness) of ICSRs in accordance with client conventions/guidelines and Standard Operating Procedures.
Education and Skills:
l Degree in Science
l Good knowledge of medical terminology
l Fluency in written and spoken English and Japanese
l Computer proficiency, an ability to work with web-based applications
l Capability to make concise, accurate and relevant synopses of medical text and data, and the ability to write unambiguous medical text
l Ability to evaluate data and draw conclusions independently
l Typing and transcription accuracy