工作內容

Job Overview:  

 

The Senior Statistical Programmer is responsible for all aspects related to programming activities for the data preparation and analysis of clinical data. Duties include creating all datasets, tables, listings and figures according to the specific project Statistical Analysis Plan (SAP) as well as coordinating Quality Control efforts and implementing all programming required for study/project completion.  

 

Job Duties and Responsibilities: 

 

Development and documentation of programs used in the production of computer generated outputs for clinical study reports, registration and submission documents, publication requirements plus any other document used to present clinical trials data, e.g. answers to requests from health authorities, individual sponsors requests, scientific papers and conferences, etc. in line with existing regulatory guidelines, industry standards and standard operating procedures issued by Clinipace and/or clients as appropriate. 

 

Conception and generation of dataset specifications 

 

Design of integrated databases and development of mapping specifications for integrated datasets 

 

Development and documentation of programs used to generate datasets 

 

Development and documentation of programs used to generate listings, tables and graphs 

 

Program validation including generation of validation documentation 

 

Data preparation and documentation according to CDISC data standards 

 

Preparation of electronic submission of clinical data 

 

Intense and crossfunctional interaction with other members of the project team 

 

Providing internal consultancy in various review activities like database design, data validation rules, analysis plans, table shells etc. 

 

Interaction with clients 

 

Design, development, documentation and validation of tools and macros to continuously improve quality and efficiency of processes applied 

 

Writing of User Manuals 

 

Training of group members on new processes, programs etc. as appropriate 

 

Initial Training on existing processes, programs etc. for new group members 

 

Attending and representing the company at business conferences 

 

Participation in industry working groups 

 

Coordination of allocated teams of Statistical Programmers assigned to a specific client project including the monitoring of workload, estimation and forecast of resource needs within the specific activity and responsibility for coaching and education of other team membersCoordination of internal projects for continuous improvement of processes and systems

發展願景

At Clinipace, a global, full-service contract research organization (CRO), our approach to clinical research is personal. We deliver a level of collaboration and flexibility not possible in a traditional CRO environment. With personalized services and solutions, local regulatory expertise and therapeutic leadership, we overcome the most difficult industry challenges across all major therapeutic areas including oncology, gastroenterology, nephrology and urology, rare disease, and women’s health. We strive to improve the way clinical research is performed and impact the future of health care using the most advanced technology and a CHALLENGE ACCEPTED approach.

成就樂趣

丘以思生技(Clinipace, Formerly Choice Pharma)為美商公司,專精臨床試驗,在業界擁有優良商譽。待遇福利佳,除享勞保,健保,員工團體保險,車資補助,員工意外險,生育、婚喪補助金外,並有優秀的工作團隊及完整的教育訓練。在休假方面,除週休二日外,並有彈性工作時間、遠優於勞基法的年休假制度。是一個可以學習成長、獲取工作成就感的溫暖大家庭。

工作制度/性質

工作地點:
台北市 信義區 松仁路101號10樓A,D,E室    [地圖]
工作時間:
日班
休假制度:
週休二日
工作待遇:
面議(經常性薪資4萬含以上)    [$薪資公秤]
工作福利:
[同公司福利]
公司福利 ×

法定項目
勞保、健保、週休二日、陪產假、育嬰假、生理假、特別休假、員工體檢、勞退提撥金

福利制度
獎 金 類:年終獎金
保 險 類:員工團保
餐 飲 類:伙食津貼
娛 樂 類:國內旅遊、國外旅遊、春酒、下午茶、家庭日
丘以思生技(Clinipace, Formerly Choice Pharma)為美商公司,專精臨床試驗,在業界擁有優良商譽。待遇福利佳,除享勞保,健保,員工團體保險,車資補助,員工意外險,生育、婚喪補助金外,並有優秀的工作團隊及完整的教育訓練。在休假方面,除週休二日外,並有彈性工作時間、遠優於勞基法的年休假制度。是一個可以學習成長、獲取工作成就感的溫暖大家庭。


工作性質:
全職
職務類別:
檔案資料管理人員 統計學研究人員

要求條件

身份類別:
一般求職者
工作經驗:
不拘
學歷限制:
大學以上
科系限制:
醫藥衛生學門 數學統計學門

語言能力:
英文 聽-精通 | 說-精通 | 讀-精通 | 寫-精通

附加條件:

Education 

BSc, MSc or equivalent experience in information technology, mathematics, statistics or medical documentation 

 

Experience 

Minimum of 5 years experience in processing and analysing clinical trial data or demonstrated aptitude for statistical programming work

profile
聯絡人員:
HR

需求人數:
1人
到職日期:
不限

面試地址:
郵寄地址:
傳真號碼:

電子信箱:

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