Statistical programmer/Clinical SAS Programmer

Summary: DataTek, Inc. is a global IT consulting firm that provides technology solutions for Fortune 500 companies. They are seeking a Statistical Programmer/Clinical SAS Programmer to provide programming support for clinical trial data reporting and regulatory submissions, while collaborating with the programming and statistics team. Responsibilities: - Provide programming support for clinical trial data reporting and regulatory submissions - Support the Programming and Statistics lead - Integrate summaries of efficacy and safety - Demonstrate SAS programming skills - Participates in statistical team and some project team interactions - Provides timely and effective communication to the programming and statistics leads - Perform queries, identify data patterns, generate reports and charts - Provide analysis and testing for accurate data collection and statistical modeling - Perform data collection, data manipulation, data quality control and statistical analysis using SAS language, procedures and Macros - Creates statistical programs using SAS to generate or Validate TLFs and derived datasets for regulatory submissions - Performs and documents programming validation of TLFs, and derived data sets created by other programmers and/or statisticians - Performs ad-hoc programming requests as required to support the Clinical Development department - Creates and maintains SAS Macros to create standard formatted output and assist with automation of routine tasks - Creates, validate and documents mapping specifications for derived datasets Required Qualifications: - Provide programming support for clinical trial data reporting and regulatory submissions - Support the Programming and Statistics lead - Integrate summaries of efficacy and safety - Demonstrate SAS programming skills - Participates in statistical team and some project team interactions - Provides timely and effective communication to the programming and statistics leads - Perform queries, identify data patterns, generate reports and charts - Provide analysis and testing for accurate data collection and statistical modeling - Perform data collection, data manipulation, data quality control and statistical analysis using SAS language, procedures and Macros - Creates statistical programs using SAS to generate or Validate TLFs and derived datasets for regulatory submissions - Performs and documents programming validation of TLFs, and derived data sets created by other programmers and/or statisticians - Performs ad-hoc programming requests as required to support the Clinical Development department - Creates and maintains SAS Macros to create standard formatted output and assist with automation of routine tasks - Creates, validate and documents mapping specifications for derived datasets - MS/PhD degree S.T.E.M majors, but prefer in statistics, biostatistics, applied statistics, mathematics - Minimum one year experience including academical experience required or equivalent training - A Master's or PHD degree with a major in Statistics, Applied Statistics, Biostatistics, Mathematics', Biology, S.T.E.M and any related to field - Must be great team player - Must be able develop positive working relationships - Need to have good analytical and problem-solving skills - Must have high level of motivation/self-starter work ability - Must work independently as well as collaborate in teams - Remote: Relocate before starting work (Required) Preferred Qualifications: - Master's (Preferred) - Sponsor H-1B and GC, but prefer permanent resident and US citizenship Required Skills: SAS programming, Statistical programming, Statistical analysis, Data manipulation, Data quality control, Statistical modeling, SAS Macros, Clinical trial data reporting, Regulatory submissions, Analytical skills Benefits: Sponsor H-1B and GC, but prefer permanent resident and US citizenship, Holiday and Vacation pay, Medical, Dental, Vision and Life insurance, 401K Retirement plan