晉加股份有限公司
統一編號
16320346電話
傳真
公司網址
http://www.statplus.com公司位置
產業類別
產業說明
CRO
About公司簡介
StatPlus, Inc., a leading contract research organization was founded in 1998. StatPlus distinguishes itself from its competitors in the services of high quality, speed, and excellence.
The StatPlus staff of experienced clinical scientists, statisticians and data managers work as a team to deliver high quality products. In addition, a number of distinguished medical consultants are on staff providing technical guidance and supervision in various therapeutic areas.
At StatPlus, our mission is to provide high quality services, which include biopharmaceutical applications in the areas of clinical research to our clients, on time and on budget. We commit to accomplish this mission with innovation, integrity and excellence
‧1998: Company formed and provided full services for Clinical Research
‧1999: Received 1st Taiwan DoH GCP Inspection
‧2000: Provided services for US clients in statistical analysis
‧2005: Attended US FDA site inspection in Taiwan
‧2007: Submitted US FDA IND Study
‧2009: Conducted H1N1 Flu Vaccines Studies in Taiwan
‧2011: Formed Asia CRO Alliance including China, India, Japan,Korea, Malaysia, and Taiwan
The StatPlus staff of experienced clinical scientists, statisticians and data managers work as a team to deliver high quality products. In addition, a number of distinguished medical consultants are on staff providing technical guidance and supervision in various therapeutic areas.
At StatPlus, our mission is to provide high quality services, which include biopharmaceutical applications in the areas of clinical research to our clients, on time and on budget. We commit to accomplish this mission with innovation, integrity and excellence
‧1998: Company formed and provided full services for Clinical Research
‧1999: Received 1st Taiwan DoH GCP Inspection
‧2000: Provided services for US clients in statistical analysis
‧2005: Attended US FDA site inspection in Taiwan
‧2007: Submitted US FDA IND Study
‧2009: Conducted H1N1 Flu Vaccines Studies in Taiwan
‧2011: Formed Asia CRO Alliance including China, India, Japan,Korea, Malaysia, and Taiwan
Product/Service產品/服務
臨床試驗研究委託服務
Benefits公司福利
法定項目
勞保
健保
週休二日
生理假
特別休假
勞退提繳金
福利制度
獎金類
員工生日禮金
三節獎金
休假類
不用補班
餐飲類
誤餐費
娛樂類
國內旅遊
國外旅遊
尾牙
補助類
員工結婚補助
生育補助
員工及眷屬喪葬補助
其它類
員工在職教育訓練
注意！本區全部福利項目可能依不同職缺有所不同，實際職缺福利請依面試時與公司面談結果為準
Resources其他資源
Jobs工作機會
共 5 個職缺
工作性質(不拘)
職務類別(不拘)
工作地區(不拘)
每頁 10 筆
07 / 17
General Description:
Develop clinical trial related documents for submission to regulatory authorities and/or IRB.
Clinical documents, including but not limited to:
1. Clinical study protocols and amendments,
2. Investigator brochures,
3. Clinical study reports,
4. Regulatory briefing documents,
5. Informed consent form
6. Clinical sections of INDs, NDAs, and
7. Other regulatory/IRB submission documents.
07 / 17 ｜ 已被閱覽 200+ 次 ｜ 1~5 人應徵
台北市信義區
月薪 60,000 元以上
碩士、博士
3 年以上經驗
07 / 17 ｜ 已被閱覽 200+ 次 ｜ 1~5 人應徵
07 / 19
The Biostatistician is responsible for all the tasks of statistical analysis in clinical studies including the statistical analysis plan, statistical report, analysis datasets, TFLs output, and the corresponding SAS programming. Supervise the programmer to complete the production of datasets and analysis outputs. Oversee the progress of data management and statistical analysis for projects. Works under the supervisor of the director of the technical department to ensure the quality of statistical analysis and all the tasks that are delivered on time and within the scope and also provides statistical advice to sponsor and project team.
07 / 19 ｜ 已被閱覽 200+ 次 ｜ 1~5 人應徵
台北市信義區
待遇面議
碩士、博士
經驗不拘
07 / 19 ｜ 已被閱覽 200+ 次 ｜ 1~5 人應徵
The Clinical Data Analyst is responsible for scientific programming in data validation, dataset transformation, and statistical analysis programming. Also, the Programmer supports data management or statistical activities for projects, if needed.
Qualified individuals must have a bachelor‘s degree in statistics, biostatistics, mathematics, public health, or related field, or have 0-2 years of pharmaceutical experience in drug research and development. An advanced master’s degree is preferred. Knowledge of Statistical Application Software (SAS) or other programming language is required. The knowledge of Clinical Data Interchange Standards Consortium (CDISC) standards is preferred.
無工作經驗者月薪36000~42000元
07 / 17 ｜ 已被閱覽 300+ 次 ｜ 1~5 人應徵
台北市信義區
月薪 36,000 至 50,000 元
碩士、博士
經驗不拘
07 / 17 ｜ 已被閱覽 300+ 次 ｜ 1~5 人應徵
The Data Manager is responsible for all clinical data management tasks, database design, EDC construction, status report preparation, and supports scientific programming.
Qualified individuals must have a bachelor‘s degree in statistics, biostatistics, mathematics, nursing, epidemiology, or related field, or have 0-2 years of pharmaceutical experience in drug research and development. Knowledge of Statistical Application Software (SAS) or other programming language is required. The knowledge of Clinical Data Interchange Standards Consortium (CDISC) standards is preferred.
無工作經驗者月薪28590~32000元
07 / 17 ｜ 已被閱覽 300+ 次 ｜ 1~5 人應徵
台北市信義區
月薪 28,590 至 45,000 元
大學以上
經驗不拘
07 / 17 ｜ 已被閱覽 300+ 次 ｜ 1~5 人應徵
07 / 17
臨床試驗監測、臨床試驗相關資料整理歸檔、協調臨床試驗相關人員與事務、臨床試驗專案管理、解決問題
無工作經驗者月薪38000~45000元
07 / 17 ｜ 已被閱覽 600+ 次 ｜ 1~5 人應徵
台北市信義區
月薪 38,000 至 60,000 元
碩士、博士
經驗不拘
07 / 17 ｜ 已被閱覽 600+ 次 ｜ 1~5 人應徵
晉加股份有限公司