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本帖最后由 excelhr 于 2010-1-8 11:37 编辑
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2 r- _) m) ?: DWe will offer you an attractive pay, promotion space and help you to develop your career...6 Q: R* ]' ]6 `
Position:Sr.Statistical Programmer/Statistical Programmer
9 Q" ]4 z! L" yLocation: Shanghai / Beijing China2 y: |6 n* Z4 J& `! y# s$ G. E
3 c) r( I* P8 \$ ]4 o2 L) l7 jResponsibilities
+ r( L" a5 a. `; \& u- G Develops SAS programs to produce data listings and Case Report Form Tabulations (CRT) as by domain or by subject
. V# j2 d( y! n Builds standard tabulation datasets according to certain industry standard or the client’s requirements
" Q F0 G3 [2 _+ \ Creates derived or analysis datasets according to certain industry standard or the client’s requirements based on the statistical analysis plan5 `2 D6 c P0 {: y0 ^% ^% h
 Reviews the standard tabulation datasets and/or analysis dataset development specifications and SAS programs created by other SAS programmer(s)
% v! U$ Z& O& k& X1 f0 ^ Develops SAS programs to implement statistical analyses and generate tables, listings and figures as specified in the statistical analysis plans
3 z' M, k: t6 h9 n) ~ Performs validation of and quality assurance aspects of all SAS programming activities, C _* z, ^, ?
 Supports for regulatory submission (e.g. NDA and PMA) including submission datasets preparation
- U1 ]; j% g! R! v Develops SAS programs for other needs1 S* P( q. M# y7 K# w
 Represents SAS programming team at project team meetings and provides updates to project team on status of tasks/ n; q/ ?3 w8 U8 ~& m; j {- A( T+ w
 Communicates with project team members such as Project Biostatistician, Data Manager, and Project Manager regarding project issues8 G, _3 A( k9 V' |1 [
 Communicates with client regarding SAS programming issues
& T8 Y2 O2 K- ~1 s. y1 g Ensures integrity of all systems by preserving security and following change control procedures
( W0 Q) C7 G& l. e1 H Participates in department level applications such as SAS Macro Library Development
" p1 p2 _/ ?/ `! B2 e& Z Consults on other statistical programming tasks, such as support for CRF design, database development, data validation plan and blinded data review: p4 |. E% h# J# U3 Q* ^: ?+ L: F
 Consults on SAS program design strategies and provides technical support to programming team9 C, a8 p% Y4 i$ s4 e& z) P
 Mentors and trains low level biostatisticians and new colleagues% H# R# T1 X4 q3 N1 s8 N4 T. v
 Performs other duties assigned by supervisor
& A7 e+ M9 O: k- iQualifications
' q. W3 j) S _- } c+ u0 }& n" ^- p Bachelor degree in a scientific or technical area (statistics or related subjects is preferred); An advanced scientific degree is desirable6 X2 s/ w/ d- Q: m4 r% u7 X3 x
 Knowledge of programming methodology; a high degree of skills in the management and resolution of SAS programming issues+ u- @: y7 I% y, a' O8 g4 R
 At least 3 years (for bachelor) or 2 years (for master or above) experience with Base SAS (data step programming), SAS/SQL, SAS/MACRO, SAS/ODS, SAS/GRAPH, SAS/ACCESS and SAS/STAT. ISS/ISE experience is a plus
) S2 A, w) p2 v! w4 \/ A Experience with the CDISC data standards and clinical database setup is preferred7 v t2 s4 Y3 t: q6 m
 Experience of international drug development in a multicultural environment is a plus
1 C; C7 `9 p2 l+ p8 l" s Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
! K1 u( I6 X, W+ X Demonstration of ethical leadership skills and exhibit high moral character so as to foster respect for ethnic and religious diversity and support equal opportunity for all employees based on demonstrated ability and to exhibit a high degree of skills in the management and resolution of conflict
9 n: T: C: q! G2 N' {# h% c9 K Knowledgeable in all aspects of the drug agencies (e.g. FDA) regulations and requirements governing the conduct of drug, biologic and device studies including, but not limited to, GCP and ICH requirements' \* l; l4 O: B3 a4 ?2 H
 Excellent communication and interpersonal skills) M1 Z6 [7 t+ ^. f& L" ^1 e
 Able to make effective presentations in public settings/ m7 E0 i$ G- I
 Proficient working in a PC/Windows environment2 l8 M: D* E7 W- Z
 A good command of English language if one’s native language is not English
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6 H8 k4 B3 h* G* EEmail:! P0 I/ J1 @ U7 E3 F
Shanghai:yujie.ma@excel-cro.com Tel: 86-21-53834000 ext.160
) y8 Z1 x$ g4 C2 t) d% h7 [Beijing: yan.li@excel-cro.com Tel:86-01-82250022 ext.211
. u$ S0 m ~( E. n$ b Z! o
5 q" Y1 g9 h+ pCompany Profile:
! u" d- C% S$ N1 j5 N, @3 c% z% a- g. h6 v
Excel-a PPD company, a leading CRO in China, was founded in Beijing in 1999, and in the last eight years it has grown into a full service CRO providing comprehensive regulatory, clinical research and quality assurance services in the areas of clinical drug development, Phase I~IV, bioequivalence studies, clinical monitoring, project management, patient recruitment, data management, biostatistics analysis, translation, medical report writing and other related services.
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" y) ~! E0 H) X2 ZExcel has successfully conducted over 125 clinical trials (phase I to IV) and has obtained nearly 200 regulatory approvals. As one of the few CROs in China using Oracle and SAS for clinical data management and biostatistics analysis, our biometrics services are being developed to comply with US FDA 21 CFR Part 11 requirements. 7 u' I9 T- ]! `( R% N
& z3 D1 O( `5 R6 E+ F/ ]Our clients currently include many of the top international pharmaceutical companies and many leading biotech companies. |
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