Please send resume to Nalin.jetty@shstinc.com
Position: SAS Developer
Location: Wayne, PA
Duration: 12 months
Location: Wayne, PA
Duration: 12 months
Minimum of a Bachelor's degree
Minimum 6 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries. Preferred Skills
Extensive knowledge of Base SAS, SAS/GRAPH, SAS/STAT, and ODS
Experience working with heterogeneous data structures
Ability to work independently and adept at managing multiple competing tasks
Good understanding of clinical data and pharmaceutical development
Knowledge and experience using SDTM and ADaM,data structures
Knowledge of FDA and ICH guidance
Knowledge of clinical trial conduct and the data and reporting requirements for clinical trials
Minimum 6 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries. Preferred Skills
Extensive knowledge of Base SAS, SAS/GRAPH, SAS/STAT, and ODS
Experience working with heterogeneous data structures
Ability to work independently and adept at managing multiple competing tasks
Good understanding of clinical data and pharmaceutical development
Knowledge and experience using SDTM and ADaM,data structures
Knowledge of FDA and ICH guidance
Knowledge of clinical trial conduct and the data and reporting requirements for clinical trials
Knowledge of SAS programming techniques needed to produce outputs in accordance with specifications The Clinical SAS Programmer creates SAS programs in support of sponsor's clinical trials according to SOPs and guidelines. This programmer will create, document, validate, process, and maintain statistical programs and macros that generate analysis datasets, tables and graphics with high quality per agreed timelines. For the project lead position, the Clinical SAS Programmer will provide direction and oversight to programmers in creating sponsor deliverables.
Act as lead programmer to write SAS programs that produce analysis datasets (ADaM) and analyses specified (ADaM) in the Statistical Analysis Plan • Act as quality control programmer to validate SAS programs that produce analysis datasets and analyses specified in the Statistical Analysis Plan • Assist the Manager of Clinical programming in overseeing the daily tasks associated with clinical programming and subsequent analysis to ensure sponsor deliverables are created per agreed timelines and to high quality standards. • Ensure SAS programs adhere to SOPs, guidelines, and specifications • Ensure SAS program output matches the requirements of the Statistical Analysis Plan • Consult with managerial, statistical, data management, DIS, and medical writing personnel to clarify program intent, identify problems, and suggest changes. • Design and/or review database structure • Create derived-analysis datasets • Execute analyses specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plan (RAP) under the guidance of the project statistician • Take instructions and perform tasks as necessary as directed by reporting manager • Ensure specifications and documentation are correct and complete • Work with other team members to ensure outputs are correct and complete • Organize, plan, and prioritize work to develop specific goals and plans to prioritize, organize, and accomplish project objectives • Analyze information and evaluate results to choose the best solution and solve problems.
Thanks & Regards,
Nalin Jetty,
Sr. Recruiter
Seven Hills Software Technologies Inc
412-450-1316 Ext 105
Nalin.jetty@shstinc.com
http://www.shstinc.com
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