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Statisticians /SAS Programmer(Shanghai ) 1 s+ A. Z( f, l. ]
2 ]: c' H' P8 `% i& ~0 s. R$ O
4 q- E( S( g! s, J2 |: W! F& sResponsibilities; s! i. J. \, Q- n+ j% ?
• Participate in setting up a study including the development of statistical methodology, fill up the statistical section of study protocol, perform sample size estimation, and carry out randomization procedure# ]/ F* r* O8 c" y+ z
• Develop SAS programs to create statistical tables, listings, and graphics according to the statistical analysis plan H/ H3 K; s/ [5 v6 ?
• Perform quality control and/or second program validation of other programmers’ programs.4 c* m- F% F) N. J5 Q8 s$ q* Z
• Participate in CRF design, review , database setup, data validation and ensure that all critical contents are included0 k9 I; m w3 V/ L; e0 l6 P
• Develop statistical analysis plan, data validation plan, data management plan and blind data review
3 {. T' i. g: }& h• All other duties as assigned
9 n+ x. J: k- K$ j" |2 S; `
F" h! S1 s" c; q- f' HQualifications:
4 o& g+ Z; M/ d7 x• Graduate degree in public health, Biostatistics or related disciplines6 q8 k( \8 }( L4 P, o1 [- t
• At least 1 year experience of statistical analysis in a pharmaceutical or CRO setting
d' D" z ^- k T• Excellent communication and interpersonal skills
# t! c- Y' I4 x! T& l! g7 C• Knowledge of ICH GCP and China GCP+ c/ D3 P: r, p! M3 i8 G
• Rich experience of SAS programming, 2 years experience of SAS programming would be preferred
7 H% d9 Y9 w% S6 W; [8 Q) G• Being fluent in spoken and written English with CET-6.
% S# s8 C O9 V• Be able to work independently and complete a high volume of work
. P6 D3 h1 g- [3 }; q4 \' ?, c- j5 c% l1 \. V' K8 Y
Pls send mail to sarahsheng1003@gmail.com for more detail. |
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