Lead SAS Programmer
Job Requirement:
?  Leads the reporting project team and coordinates the development and delivery of safety
and efficacy reporting deliverables, delegating to other scientific programmers for large
and complex projects.
?  Establishes and drives reporting timelines for assigned project(s). Estimates resource
needs and procures appropriate scientific programming resources.  
?  Ensures reports and analysis package is available in a timely manner5.Stays abreast of
current data collection, data derivation, reporting and process standards; enforces use of
standards to ensure program-wide efficiencies and consistency across safety and efficacy
reporting.
?  Drives  global  and  therapeutic-area  SDTM+  and  reporting  implementation  standards
including safety and efficacy.  
?  Collaborates with peers to maximize global consistency.  
?  Collaborates  with  and  provides  input  to  vendors/partners  to  ensure  that  externally
collected data effectively supports regulatory analysis and reporting.  
?  Understands  business  drivers  and  needs;  translates  them  into  designs  to  achieve
technical solutions.
?  Accountable  for  the  creation  of  specifications  for  regulatory  reports  and  statistical
analyses. 9.Owns validation documentation.
?  Ensures adherence with departmental SOPs and guidelines.
?  Provides input to CDR SDTM & views, collector design & edit checks and data integrity
reports to ensure that report deliverables are accurate and complete.
?  Serves as leader of cross-departmental and strategic teams dedicated to process issues.
?  Provides  instruction,  training  and  mentorship  to  less  experienced  staff  regarding  all
aspects of the function.  
?  Participates in the development of the training materials. Mentors junior staff members on
publishing in statistical computing journals.
Job Qualification:
1) Must haves  
??Excellent written and oral communication skill (English).  
??Able to demonstrate a strong understanding of CDISC standards. Experience with SDTM
programming with FDA submission experience.  
??At least 3 years within a leadership role. Able to manage and communicate team time lines.  
??Experience in writing and adhering to SOPs.  
??Able to demonstrate strong knowledge of particular SAS programming skills such as  
??Macros  
??SQL  
??SAS Graph  
??Proc Report  
2) Nice to haves  
??Work experience with a US company.  
??Experience with ADaM programming.  
??Educated in US.  
??SAS certification  
??Microsoft certification  
??Unix experience.  
3) Experience level
??10+ years of SAS programming experience.  
??5+ years Clinical SAS programming experience.  
??BA/BS degree in computer science, statistics, mathematics or related science.  

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