Position Description:

Sr. Statistical Programmer Analyst for Medtronic, Inc. Minneapolis, MN.Provide clinical and statistical knowledge and software programming expertise as part of the Statistical Programming team to develop and maintain software programs and process methodology which meet internal and external clients’ needs, including clinical research study support. Plan and coordinate the development of solutions for projects primarily using SAS® software such as Base SAS®, SAS/STAT, SAS Macro language, SAS/SQL, and SAS/GRAPH on multiple platforms including personal computer or server based platforms. Gather and ensure quality of clinical data and integrate data from multiple sources. Coordinate closely with statisticians and biostatisticians on clinical analysis. Prepare data for regulatory submission in accordance to clinical data standards including Clinical Data Interchange Standards Consortium (CDISC), Clinical Data Acquisition Standards Harmonization (CDASH), and Study Data Tabulation Model (SDTM) for electronic submissions. Coordinate clinical database analysis programming utilizing SAS on multiple platforms for programming, testing, documenting, and validating statistical programs and tools per Food and Drugs Administration (FDA) and Pharmaceuticals and Medical Devices Agency (PMDA) requirements. Position is open to telecommuting from anywhere in the United States.

Basic Qualifications:

Masters’ degree or foreign equivalent in Computer Science, Computer Engineering, Information Technology Management, Biostatistics, Statistics or related health / engineering field and two (2) years of experience as a statistical programmer, biostatistician, or related occupation in SAS® programming. Or, a Bachelors’ degree or foreign equivalent in Computer Science, Computer Engineering, Information Technology Management, Biostatistics, Statistics, or related health /engineering field and five (5) years of experience as a statistical programmer, biostatistician, or related occupation in SAS® programming. Must possess a min. of two (2) years’ experience with each of the following: Base SAS®, SAS/STAT, SAS Macro language, SAS/SQL, and SAS/GRAPH; Working with clinical data and integrating data from multiple sources; Working with statisticians and biostatisticians on clinical analysis; Preparing data for regulatory submission in accordance to clinical data standards including CDISC; Clinical database analysis programming utilizing SAS; Programming, testing, documenting, and validating statistical programs and tools per FDA and PMDA requirements.

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