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University of Rochester Analyst/Programmer Sr - 235248 in Rochester, New York

Analyst/Programmer Sr Job ID 235248

Location School of Medicine & Dentistry Full/Part Time Full-Time Favorite Job Regular/Temporary Regular Opening

Full Time 40 hours Grade 054 CCRC

Schedule

8:30 AM-5 PM

Responsibilities

General Purpose:

Analyzes problems, provides program specifications, and develops or modifies programs with major emphasis on statistical analysis techniques with considerable latitude for independent judgment. Statistical techniques focus on the analysis of longitudinal health-related data including data derived from complex FDA regulated and non-regulated clinical trials.

Responsibilities:

  • Plans and performs complex statistical analysis of cardiologic research data. Includes data management and programming in statistical packages such as SAS.

  • Designs, maintains, tests and verifies complex SAS programs, SAS macros and databases with a strong focus on quality control measures to prepare for extensive data analysis and presentation

  • Consults with collaborating researchers including doctors, programmers and biostatisticians, to assess data preparation, transfer, management, program design, testing, software package selection, and use of systems software/hardware. Offers solutions and suggestions to provide optimum efficiency and cost effectiveness

  • Designs, maintains, and verifies complex programs and databases with a strong focus on quality control measures to prepare for extensive data analysis and presentation.

  • Keeps abreast of trends as they relate to statistical analysis methodology and software by self-study, attending job related seminars, courses or conferences that enhance personal development and strengthen user function

Requirements:

  • Bachelor’s degree in related discipline such as computer science, business mathematics, statistics, science or engineering required

  • Master’s degree in any of the disciplines listed above preferred

  • 3-4 years of related experience, preferably 1-2 years in a supervisory capacity required;

  • 4+ years of related experience preferred;

  • Strong experience in statistical programming in SAS preferred;

  • Or equivalent combination of education and experience required

  • SAS Macro and SQL skills and experience preferred;

  • Operating in FDA/HIPAA regulated and/or validated environment with particular emphasis on clinical research background preferred;

  • Excellent attention to detail, organizational and interpersonal skills required, with the ability to work collaboratively in a team environment preferred

    How To Apply

All applicants must apply online.

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