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工作地点:
+ X3 U0 _5 l! }: @上海" n) P6 e- L6 ~6 T
薪金:5 z) b+ H' f+ @6 K( K
年薪20-50W+ e% K. D' |+ I
招聘岗位:
3 L0 D& B9 x! a% O) a( O# hBiostatistician. e9 k. @6 k6 S4 y! r
联系方式:/ O" V. d6 s5 a5 P: i0 M
jerryyoung6@网易163邮箱* z* q6 L! n1 M8 Y3 f
! V9 y# b6 d; I# FAccountabilities
- D9 }; z* {; K( H2 `; cDevelops statistical analysis plans and reporting specifications for simple to moderate clinical studies.
6 T: Y+ {2 O z: s0 ?• Develops and describes appropriate statistical techniques for the analysis of data in a statistical analysis plan. 5 r2 H$ X2 h1 @" W
• Works with other statisticians on statistical methodology, study design, therapeutic area details, and data analysis.
; I% u8 z% d% [3 J, Z7 M' T• Design appropriate shells and specifications for outputs. 9 c, c( t* i3 O8 z( i4 R) Q
Performs statistical analyses and interprets results from simple to moderate clinical studies. % D8 E" z3 a: l- H
• Develops or QCs analysis programs to implement techniques described in the statistical analysis plan.
! e$ u! ? H5 g4 O7 E+ m' P• Approves final database for freeze/lock. ) F! w; Y1 T. r8 A1 k
• Assesses model assumptions for statistical analyses. + a& {' Z* J/ |- s* R# E x
• Works with programmers, writers, and clinicians to coordinate data summarization and analysis activities, including summary statistics, tabulations, graphics, analysis output, and raw data listings. ) \8 k; Z+ y3 `& a2 n: \0 H8 V8 X
• Develops and reviews statistical reports and statistical sections of clinical study reports. ! d4 ^" n+ c; r7 w: r
Contributes statistical expertise to project teams for the design, analysis, and reporting of simple to moderate clinical studies.
( ] ]. w! @3 U( M/ [5 O• Serves as primary functional representative on project teams.
2 i/ G: d! d- p! V& H• Provides input into the preparation and review of clinical study protocols.
( g, l3 N1 i' u- x3 y2 t2 j1 n( f• Creates dummy and final randomization schemes for clinical studies. 3 a( C5 ~, c. H( P5 x# K5 p/ e: c
• Participates in the development and review of CRFs, data edit specifications, and critical variable lists.
1 P+ h, E: I% m0 G• Works with the project manager and functional manager to determine resource projections and project schedules.
' |) G X3 I; k; @, i• Visits clients to discuss statistical issues.
; k% [0 Y& c; o7 o0 OMaintains, develops, and shares knowledge of company and industry procedures and methodologies. 9 D# L4 z/ F* H `
• Performs billable work in accordance with WuXiPRA’s policies, procedures, and SOPs.
8 r# E8 @+ B* J v! `• Maintains solid knowledge of drug development process.
, d! x/ l0 x8 y, f• Maintains solid knowledge of SAS procedures and good programming practices.
0 y4 x5 G6 z. \2 D* Y1 U, j• Continues statistical training on new methods and techniques via self-study, internal training and courses, and external conferences and courses.
5 u; F# M- A; e5 W• Trains and mentors new or junior statisticians on statistical methods and WuXiPRA procedures.
$ N6 z4 ?: Q; g4 U• Develops knowledge of FDA and EMEA guidelines and requirements for reporting of clinical trials data. 4 K A% a6 n1 ?7 Q
0 [$ W2 W1 L7 Q1 W9 ~& DQualifications
+ h" m, Y& Z, q3 H8 \' B+ `2 V' Q4 | MS degree with 3 years of experience within the clinical trials or pharmaceutical industry or PhD degree in statistics or biostatistics
- @- m! G7 r i. B: y2 n0 _* C- b Demonstrated expertise in multiple and complex statistical areas
; A( O* d! w+ v E/ _ Demonstrated ability to plan, implement, and monitor the statistical processes for clinical studies 4 r( l9 x0 P0 r* M& |/ j9 v- _# f
 Excellent written and oral communication skills; Read, write and speak English. & Z8 w" E7 }; f
2 {$ F2 C+ n: Q) _/ M
If interested in this position, please send your English CV to jerryyoung6@网易163邮箱 |
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