*Hi**,*
*Hope you are doing great!!* * Please find the requirement below **,* *If you find yourself comfortable with the requirement please reply back with your updated resume with details to this email id s.dak...@esskay-inc.com <s.dak...@esskay-inc.com> and I will get back as soon as possible.* *Position: SAS **Programmer Analyst* *Location:* * South Mounds View, MN* *Project Duration: 12+ months* *Job Description:* This is a statistical programmer/analyst position, programming in SAS every day. Tasks may include production and validation programming for clinical reports (e.g., tables, listings, and graphs), creating SAS datasets and SAS analysis datasets (can merge from multiple sources and create derived variables), ad-hoc listing (e.g., to help with data cleaning), and creating study management reports (e.g., data quality report). Work will be done according to standard operating procedures for development and documentation of work. Industry experience is a must. (Pharma, research institutes, clinical, medical facilities) This is not a data management role. It is more analysis and reporting centered. Candidates must possess leadership abilities, work within a team environment and be open to other duties as they are assigned. *Responsibilities: * - Plans and coordinates programming, testing, and documentation of statistical programs for use in creating statistical tables, graphics, and listing summaries. - Programs analysis database manipulations and transfers of data for internal and external clients. - May integrate databases from multiple studies or sources. - Develops listing and table specifications with study Biostatistician. - Interact with Data Management and Biostatistics staff and SP team members to negotiate timelines, responsibilities, and deliverables. - Understands and complies with Standard Operating Procedures and Work Instructions. - Programs, tests, and documents statistical programs and tools in accordance with SP standards and validation procedures. - Meets milestones as assigned. - Performs other duties as directed by Statistical Programming management. Will be working on CRDM trials. - Experience using *SAS for more than 2 years and using SAS on clinical trial data analysis*. - Industrial experience is preferred - Regulatory submission experience is a plus - Prefer the candidate has industry experience and had experience with PMA submission etc. - Absolute skill is SAS programming skills including *SAS BASE/STAT/MACRO/SQL etc*. *Notes:* Hiring manager prefers candidates that are able to potentially get hired on full time. Local candidates preferred. Position may potentially be extended up to 2 years total. *Required Skills:* Education Level: High School Diploma or Equivalent Program Languages: *SAS* Software Application Knowledge: *SAS* MS Excel *Program Languages: *SQL Unix Shell Script -- -- *************************************************************************************** For all SAP related tutorials,Articles,Faqs,Tips www.sapbrainsonline.com **************************************************************************************** You received this message because you are subscribed to the Google Groups "sapbrains" group. To post to this group, send email to sapbrains@googlegroups.com To unsubscribe from this group, send email to sapbrains-unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/sapbrains?hl=en --- You received this message because you are subscribed to the Google Groups "sapbrains" group. To unsubscribe from this group and stop receiving emails from it, send an email to sapbrains+unsubscr...@googlegroups.com. For more options, visit https://groups.google.com/d/optout.