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Statistical Programmer (SP)

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Onsite

Statistical Programmer (SP)

ENDPOINT DATA ANALYTICS

Statistical Programmer (SP)

Skills

Google Cloud PlatformLinux

19 days ago

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Important information


Location:

Telangana, India

Work mode:

Onsite

Published on:

1 October 2026

What they need


by Epda in Statical Programmer

On-site Hyderabad mon-fri

JOB DETAILS

Job Role Insight
  • Offered salary

    as-per industry standards

  • Career level

    Junior

  • Qualification

    Associate

  • Experience

    1 - 2 Years

  • Quantity

    2 person

  • Hiring location

    Hyderabad

Description

Overview

Provide Programming proficiency to develop and maintain programs to meet internal and external standards. Provide and assist in the development of project-related solutions to a wide range of statistical programming tasks.

Responsibilities:
  • Working to ICH GCP and other applicable industry standards
  • Review the respective study protocol/CRF
  • Creation /Review of annotated CRFs
  • Creation /Review of Data specifications
  • Develop edit checks programming per the data validation plan or data management plan
  • Write SAS programs to generate tables, listings, and figures and analysis datasets
  • Develop programming for CDISC deliverables (SDTM, ADaM and define.xml)
  • Communicate with programming and statistics leads
  • Assist in the development of programming documentation including specifications, as appropriate, under supervision
  • Reconciliation of external data
  • Perform quality control on final datasets, reports
  • Prepare and review Data Transfer Agreements
  • Develop SAS macros as needed
  • Understand and adhere to organization defined standard operating procedures (SOPs)
  • Fulfil project responsibilities at the level of assisting the statistical programming lead
Education:

Master’s / bachelor’s degree computer science or biostatistics or related field.

Experience & Skills:
  • 2-year relevant experience; or equivalent combination of education, training and experience
  • Experience in SAS programming for multiple phase clinical trials in a pharmaceutical/CRO environment
  • Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Proven experience with Unix, Linux and Windows operating systems
  • Proficient in written and oral communication
Request to send the Resume to: [email protected]

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