Statistical Programmer

V-Soft Consulting Group, Inc.

Louisville, KY · HybridJobSeen todaySeen in employer's feed today

Louisville, KYHybridJobNo compensation foundSeen todaySeen in employer's feed today

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At a glance

Compensation

No compensation found

Location

Louisville, KYHybrid

Work Authorization

Not specified

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Job overview

Statistical Programmer develops healthcare support software, programs and analyzes health‑care industry data, and creates medical data analysis streams. The role involves UNIX shell scripting, system administration, database management, and advanced statistical analyses using SAS, SPSS, and Excel within clinical trial environments, adhering to regulatory standards.

Skills & qualifications

RequiredNice to have

Skills

UnixWindows XPSoftware Development Life CycleSASSPSSExcelCC++Shell ScriptingDatabase ManagementSystem AdministrationClinical TrialsFDA Regulations

Qualifications

Bachelor's DegreeMaster's Degree or Equivalent in Biomedical Engineering Science Health or Related FieldFive Years Experience

Full job description

Minimum Education Required

Bachelor's Degree

Compensation

Hours Per Week

Number Of Positions

Job Description

STATISTICAL PROGRAMMER: Develop healthcare related support software. Programming and analysis of health-care industry data, Development of medical data analysis streams including statistical analyses, UNIX shell scripting, troubleshooting, system administration. Will be responsible for running and developing sophisticated shell scripts, advanced statistical analyses, Database management. Environment: UNIX, Windows XP, Software Development Life Cycle (SDLC), Statistical Analysis Software (SAS, SPSS, Excel), Languages - C, C++. Provide support for application development within a clinical trial environment. Work with statisticians, data managers, and other statistical programmers to deliver submission ready analysis data sets, study report tables, listings, and associate QC/QA, and documentation in oncology, Central Nervous System (CNS), medical devices and diagnostics. Adhere to company and regulatory standards and processes in all deliverables, utilizing and updating existing company frameworks. Environment: System Development Life Cycle (SDLC), Statistical Analysis Software (SAS), experience with clinical trials, Phase II and III, FDA regulations.

JOB REQUIREMENTS: Master’s Degree or equivalent in Biomedical Engineering, Science, Health or related field, or in the alternative a bachelor’s degree in biomedical engineering, Science, Health or related field of study AND five (5) years of experience in the offered position or related experience.

Place of Work

Hybrid

Requisition ID

13368

Application Email

[email protected]

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