Statistical Programmer Ii

2 weeks ago


Coimbatore, Tamil Nadu, India Algorics Full time

Job Components / Major Responsibilities:


This job description serves only to give a broad outline of the duties required and will be renewed and amended at periodic intervals.


  • Performs all SAS programming required for analysis and reporting.
  • Plan, write and execute SAS programs designed to analyse clinical trial data, including any or all of the following: analysis datasets, tables, listings and graphs.
  • Coordinate, create and maintain programming project documentation.
  • Validate and perform quality control checks on programming.
  • Maintains high productivity on projects and seeks input to increase efficiencies if needed.
  • Maintain, verify, and ensure the quality and accuracy of all assigned work.
  • Anticipate and communicate resource and quality issues that may impact deliverables or timelines to project team leader.
  • Work with Biostatistics and Data Management to resolve issues regarding the interpretation and reporting of data.
  • Comply with all applicable regulatory requirements, company standards and procedures.
  • Identify and solve technical problems and work independently on assigned tasks.
  • Assist with the transfer of deliverables to either internal or external sponsors.

Qualifications:

  • Bachelor's degree in Statistics/Mathematics/Computer Science or life science
  • At least three years of experience as SAS programmer for all clinical trial phases and demonstrate the ability to independently perform SAS programming.
  • Proficient in industry standards, CDISC data standards, ICH-GCP guidelines, medical terminology, and clinical trial methodologies.


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