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Title:Sr. Statistical Programmer
Salary:Open
Experience:0-4
Location:CA - Irvine

Description:
Provides statistical programming support for multiple clinical/preclinical research and development projects.

Responsibilities:
  • Collaborates with project biostatistician in the creation, implementation, and maintenance of execution plan accounting for timeline, resource and quality of the projects.
  • Ensures that all statistical programs comply with the programming coding standards and utilize available standard reporting systems, as well as macro utility programs.

Requirements:
  • Education or education/experience combination equivalent to a post graduate degree in Computer Science, Life Sciences, Statistics or Statistics related field.
    • Zero (0) years of pharmaceutical clinical research experience with the Ph.D. or Ph.D. equivalent
    • two (2) years of pharmaceutical clinical research experience with a masters degree or masters degree equivalent
    • or four (4) years of pharmaceutical clinical experience with a bachelors degree or bachelors degree equivalent.
  • Working knowledge of medical terminology, clinical trial methodologies, and software systems development.
  • Working knowledge of at least one scientific programming language and at least one statistical software package (such as SAS, S Plus).
  • Working knowledge of at least one database system.
  • Excellent analytical, problem solving, and computer skills.
  • Flexible, well organized, excellent verbal and written communication skills, and interpersonal skills.
  • Works well under pressure, with initiative to take on unfamiliar tasks.

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