国内最大CRO公司，诚聘Sr. SAS Programmer

国内最大CRO公司，诚聘Sr. SAS Programmer

# T9 S/ K$ q2 `9 S4 ~有兴趣者请联系 yujie.ma@excel-cro.com

4 [% h, P" d& F" [# I- p* \) SJOB DESCRIPTION FOR SENIOR SAS PROGRAMMER
: e, t0 b5 z/ X/ Z; ~% T4 YPerforms all SAS programming tasks for a given clinical study or studies involving drugs,
% \3 ^9 m4 u. n9 p* I4 ?+ _biologics and medical devices, acts as the primary point of contact for SAS programming
activities for a given clinical study or studies and ensures adherence to guidelines,
8 m1 i9 s" Q1 N# [" y- s. kmethodology and SOPs for software development in accordance with FDA, ICH, GCP and
SDLC methodology; and provides technical support to the programming team.
3 x9 A& U6 S5 U9 v/ V! j$ [       
Responsibilities
􀂾 Develops SAS programs to produce data listings and Case Report Form Tabulations
(CRT) as by domain or by subject
+ p; O8 H" ]) g% m2 K􀂾 Builds standard tabulation datasets according to certain industry standard or the client’s
requirements
􀂾 Creates derived or analysis datasets according to certain industry standard or the client’s
* K$ _$ X/ u9 `" R3 Grequirements based on the statistical analysis plan
􀂾 Reviews the standard tabulation datasets and/or analysis dataset development
) _! K3 x$ A& R. x$ D4 q. sspecifications and SAS programs created by other SAS programmer(s)
( t; V& S/ I# [5 z􀂾 Develops SAS programs to implement statistical analyses and generate tables, listings
3 ^1 D. q2 }0 Q/ Hand figures as specified in the statistical analysis plans
0 K9 e. t8 U4 ^6 p% @7 _􀂾 Performs validation of and quality assurance aspects of all SAS programming activities
% }# _1 s/ s2 }3 }1 U0 q, f! b􀂾 Supports for regulatory submission (e.g. NDA and PMA) including submission datasets
3 u3 e( O/ c3 k! b% v  y! D+ }preparation
􀂾 Develops SAS programs for other needs
+ C. v: ~3 _8 L  J' ^" _􀂾 Represents SAS programming team at project team meetings and provides updates to
/ H/ O) Q/ S. wproject team on status of tasks
: i3 F8 Q8 n: W􀂾 Communicates with project team members such as Project Biostatistician, Data Manager,
and Project Manager regarding project issues
􀂾 Communicates with client regarding SAS programming issues
􀂾 Ensures integrity of all systems by preserving security and following change control
9 P2 x& P/ K; \( P7 M" }; [' h; Hprocedures
􀂾 Participates in department level applications such as SAS Macro Library Development
  C- N9 \5 C, o2 N1 m􀂾 Consults on other statistical programming tasks, such as support for CRF design,
database development, data validation plan and blinded data review
􀂾 Consults on SAS program design strategies and provides technical support to
4 z0 Y1 ~3 @* f; gprogramming team
􀂾 Mentors and trains low level biostatisticians and new colleagues
; _8 S8 n6 t8 ]  G) t& p􀂾 Performs other duties assigned by supervisor
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' Q" J2 w* a6 d% i1 `3 y1 n, `Qualifications
􀂾 Bachelor degree in a scientific or technical area (statistics or related subjects is preferred);
An advanced scientific degree is desirable
, |3 n  r9 u  O4 p* E3 a. f! W􀂾 Knowledge of programming methodology; a high degree of skills in the management and
resolution of SAS programming issues
􀂾 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
% f- S/ Y0 J3 U5 {- W% W9 |􀂾 Experience with the CDISC data standards and clinical database setup is preferred
" s7 K2 p& y# ~􀂾 Experience of international drug development in a multicultural environment is a plus
􀂾 Ability to deal with sensitive inquiries or complaints from clients or potential clients and
to protect confidentiality
􀂾 Demonstration of ethical leadership skills and exhibit high moral character so as to foster
1 S) w% {, z5 {respect for ethnic and religious diversity and support equal opportunity for all employees
& G2 F0 I) i: W, U) @; Hbased on demonstrated ability and to exhibit a high degree of skills in the management
7 L$ E  V2 L; @6 p9 \" i/ ^: Wand resolution of conflict
􀂾 Knowledgeable in all aspects of the drug agencies (e.g. FDA) regulations and
2 t9 Q9 U3 Y3 b' N& ]requirements governing the conduct of drug, biologic and device studies including, but
not limited to, GCP and ICH requirements
3 ]7 e4 i- n9 E; j& r* r" j􀂾 Excellent communication and interpersonal skills
􀂾 Able to make effective presentations in public settings
􀂾 Proficient working in a PC/Windows environment
􀂾 A good command of English language if one’s native language is not English

看的很累，还是看不懂

sas  难呀    好像得好好学学