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Statisticians /SAS Programmer(Shanghai ) " s1 Z& h9 ]% I; O( I5 F
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1 | L8 _7 z. v* {- K$ DResponsibilities
. z' m4 v4 c4 h" ]• 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' D" [( Z; M7 i
• Develop SAS programs to create statistical tables, listings, and graphics according to the statistical analysis plan' e5 {) ]+ R3 U0 S/ R& r8 A5 C# A
• Perform quality control and/or second program validation of other programmers’ programs.2 M3 }6 Q" D) a5 g1 n1 D) y
• Participate in CRF design, review , database setup, data validation and ensure that all critical contents are included' i* j' h" Y$ B/ V" i! Q
• Develop statistical analysis plan, data validation plan, data management plan and blind data review
: h1 ?( a) C& ]7 n* x' K( x" t• All other duties as assigned
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Qualifications:
3 ]6 M, i5 l9 Z2 J• Graduate degree in public health, Biostatistics or related disciplines7 l3 s& K" ^" _; h& ?+ c' K
• At least 1 year experience of statistical analysis in a pharmaceutical or CRO setting$ J8 z b" m. r( m7 G1 Z
• Excellent communication and interpersonal skills3 l: y1 f' `" r- v. f2 r1 K; E
• Knowledge of ICH GCP and China GCP0 g5 R/ e$ W0 [; C8 s
• Rich experience of SAS programming, 2 years experience of SAS programming would be preferred: G% ~5 v% V# S8 B6 y1 r# E
• Being fluent in spoken and written English with CET-6.2 a6 c) u6 o3 x8 M' \9 {2 Y% O
• Be able to work independently and complete a high volume of work g- [" ?! P2 Y) Q9 N# Z
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Pls send mail to sarahsheng1003@gmail.com for more detail. |
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