南京招聘

职位描述：
Account Abilities:
1.Act as a Trial Statistician (TSTAT) for clinical trials with existing statistical standards.
2. The responsibilities cover, for example, writing the statistical section of the clinical trial protocol, reviewing case report forms, specifying the randomization, presenting critical statistical aspects at investigators meetings, preparing the trial statistical analysis plan (TSAP) and supervising the analyses. Participating in the writing of the clinical trial report and of publications thereof.
Support other TSTATs in their responsibilities. This covers, for example, validation and quality control efforts and preparing of documents.
3. Prepare specifications for data analyses of routine clinical trials by outside vendors and assures the compliance with the specifications by reviewing the vendors' products. Release of vendors product.
4. Assist other TSTATs in preparing specifications for data analyses of complex clinical trials and projects by outside vendors. Assist other statisticians in assuring compliance with the specifications by reviewing and releasing the vendors' products.
5. Provide necessary statistical and programming support needed for data mining and ad-hoc analyses within one or accross several trial(s).

Required Skills:
Ability to interact with internal and external bodies (specialists and non-specialists) on routine statistical-methodological issues at the trial level.
? Thorough knowledge of statistical methodology and on processing clinical trial information.
? Ability to write publications (as joint author) in clinical trials.
? Ability to identify data issues that may have statistical ramifications.
? Ability to understand statistical methodology appropriate to drug development.
? Good communication skills and ability to explain statistical subject matters.


If you want to apply this role, pls send e-mail to : Selina.Ren@docsglobal.com 举报 分享

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