[上海]高知特信息技术（上海）有限公司招聘

Cognizant (NASDAQ:CTSH) is a leading provider of information technology, consulting and business process outsourcing services. With more than 50 global delivery centers and 63,700 employees as of March 31, 2009, we combine a unique onsite/offshore delivery model infused by a distinct culture of customer satisfaction. A member of the NASDAQ-100 index and S&P 500 index, Cognizant is a Forbes Global 2000 company and a member of the Fortune 1000 and is ranked among the top information technology companies in Business Week's Info Tech 100, Hot Growth and Top 50 Performers listings. Cognizant is ranked 3rd in Fortune as "Best Employer" InfoTech Services company in 2009. Please visit our website for more details ww***om.[点击查看]
    Cognizant成立于1994年，公司总部设在美国新泽西洲Teaneck市，于1998年完成自己的独立整合，并在纳斯达克上市（股票代码：CTSH），成为股指NASDAQ100中唯一的全球性IT服务公司。我们为世界前2000强企业提供全面的应用软件外包业务、业务流程、咨询服务以及系统集成服务，并已率先通过ISO 9001和5级SEI CMM认证。截止2009年3月，Cognizant在全球拥有50多个交付中心，员工超过63,700人。我们不仅有完善系统的内部培训机制，并不断为优秀人才提供全球范围内on-site的工作机会。2009年，Cognizant被财富杂志评为全球员工满意度最高的公司之一。详情请登陆我们的网站ww***com[点击查看]
   

Position: Data management Specialist
   
    ROLE: Perform assigned data management activities and handles inquiries from Medical Representatives/Doctors.
   
    Time for onboard: December 2009
   
    Resource needed: 5
   
    REPORTING TO: Team Lead - Data Management
   
    ESSENTIAL QUALIFICATION:
   
    ·Graduate/Post Graduate degree with Life science/Pharmacy background (Microbiology/ Genetics/ Biotech/ Pharma/ Biochem/ Botany, etc)
   
    ·Proficient in spoken and written Japanese with good voice quality and communication skills.
   
   
   
    ESSENTIAL SKILLS/PERSONALITY TRAITS:
   
    ·Overall knowledge of Clinical Research
   
    ·Good Clinical Practice (Knowledge of GPSP would be a plus)
   
    ·ICH and Regulatory activities
   
    ·Overall knowledge of different therapeutic areas.
   
    ·Knowledge of drug development process
   
   
   
    OPERATIONAL RESPONSIBILITY:
   
    ·Review and action queries on an ongoing basis and update database based on the query resolutions.
   
    ·Respond to inquiries from MR/Dr ongoing.
   
    ·Create and maintain study CRF data standard document
   
    ·Create and maintain project and study Data Entry Instructions.
   
    ·Maintain Data Management related operational data flows.
   
    ·Review reports and take actions as defined in the DMP or eCRF review manual
   
    ·Provide listings for review to the Client as per the timelines defined in the DMP and handle discrepancies found from reviews
   
    ·Perform ongoing and final consistency checks And status reports
   
    ·Perform AE Reconciliation and query where necessary.
   
    ·Perform coding activities and raise queries where necessary.
   
    ·Document agreed discrepancies that cannot be resolved in Study Master File before clean file declaration.
   
    ·Support Quality control checks for the trail.
   
    ·Ensure delivery of quality outputs.
   
   
   
    ADDITIONAL RESPONSIBILITY:
   
    ·Participate in knowledge sharing sessions as an when applicable.
   
    ·Ensure adherence to Cognizant and Client SOPs
   
    ·Ensure timely submission of timesheets/ functional tracking spreadsheets