丘以思生技顧問有限公司

其他醫療保健服務業
  • 公司規模
    暫不提供
  • 資本額
    暫不提供資本額
  • 負責人
    暫不提供負責人
  • 公司統編
    暫不提供統一編號

公司簡介

AT CLINIPACE, IT’S PERSONAL.
With us, you get the “A” team.
We deliver a level of collaboration and control not possible in a traditional contract research organization (CRO) environment. Our goal is to guide you successfully through your clinical development program.

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.

公司位置

  • 台北市信義區松仁路101號10樓E室

產品/服務

網站位址:
https://www.clinipace.com/
相關連結:

  • Website: www.clinipace.com
  • contract research organization, CRO, pharmaceuticals, regulatory affairs, clinical trials, biotechnology, clinical development, drug development

福利制度

法定項目
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
其他類:

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。

丘以思生技顧問有限公司 工作機會(2)

  • 11/24
    面議(經常性薪資4萬含以上)
    • 週休二日
    • 日班
    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
  • 11/20
    面議(經常性薪資4萬/月含以上)
    • 週休二日
    • 日班
    Job Overview: Provides biostatistical services to meet the requirements of all Clinipace’ s clients, including full-service, Global Clinical Analytics (GCA), and other type studies. This may include but it’s not limited to: development and approval of Statistical Analysis Plans and table shells, randomization schemes, review of data management documentation, lead development of Protocols and approve the statistical section in Clinical Study Reports, serve as Quality Control Biostatistician or IDMC statistician. The Senior Biostatistician I will act independently for most projects. Job Duties and Responsibilities: Meets all the job duties, responsibilities, and requirements of a Biostatistician in addition to those listed here. Coordinate and approve Statistical Analysis Plans (SAP), table shells, programming and derived dataset specifications developed by Biostatistics and Statistical Programming staff. Lead protocol development work including experimental design, randomization, sample size calculation, statistical methods, defining study objectives and parameters. Coordinate and approve the statistical section of the Clinical Study Report (CSR) written by Biostatistics staff and collaborate with Medical Writer in preparing the integrated CSR as needed. Coordinate and approve TFL and derived datasets, programming of derived datasets and Tables, Figures and Listings (TFL), and data review and statistical analysis developed by Biostatistics and Statistical Programming staff. Provide management of other Biostatistics Department requirements and functions, such as SOP updates, as requested by line manager. Serve as Quality Control Biostatistician for sample size calculation reports. Serve as IDMC / DSMB statistician as needed. Other duties commensurate with the position as assigned by line manager. Provide staff training and study oversight as requested by line manager. Provide staff oversight as mutually agreed with line manager. More Information: https://cho.tbe.taleo.net/cho01/ats/careers/requisition.jsp?org=CLINIPACE&cws=1&rid=5037
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