Statistical Programmer – L2

1 Month ago • 2-4 Years • Programming

Job Summary

Job Description

The Statistical Programmer - L2 role is responsible for independently working on simple to medium complexity mapping activities, including SDTM/Client specific mappings for assigned clients. The role involves understanding clinical domains, mapping logic, and data issues, as well as learning the product/system for SDTM mapping. Key responsibilities include importing and exporting raw data, contributing to mapping specifications, utilizing SAS/R programming/Python programming skills for clinical trial submissions, developing programs to identify and report data issues, building CDISC/regulatory compliant datasets, and understanding CRF annotations. The programmer will also debug custom functions/SAS Macros, assist senior team members in quality control and team metrics, and communicate with internal teams and leads. This role requires adherence to company policies and SOPs.
Must have:
  • Clinical Domain knowledge
  • Familiarity with CDISC Standards (SDTM, ADaM)
  • SAS Programming (up to 2 years experience)
  • Good Communication skills
  • Learning attitude and good team player
Good to have:
  • Python Programming
  • R Programming
  • Ability to pick up multiple tools/technologies
  • Understand CRF annotations and check for consistency

Job Details

Statistical Programmer – L2

 

Job Summary:

Statistical Programmer reports to Principal Statistical programmer 3/ Lead, Statistical Programming (L4 (3) or M1), is responsible to work independently on the most of the Mapping activities (SDTM/Client specific mappings) which are simple and medium complex for assigned client in the given environment for the standard domains. Understanding clinical domain, mapping logic, data issues is a part of this role. Learning the product/system/mechanism to be used for SDTM mapping is a part of this role.

Knowledge, Skills & Abilities:

        Clinical Domain knowledge

        Familiarity with CDISC Standards (SDTM Knowledge, ADaM, Submission package)

        SAS Programming (Experience up to 2 years)

        Python Programming will be an added advantage

        R Programming will be an added advantage

        Good Communication skills, learning attitude and good team player

Education and Work Experience:

           Graduation in Pharmacy/Computer Science, or any such equivalent graduation from a reputed institute.

           Total experience is between 2 - 4 years

 

Responsibilities:

        Ability to pick up multiple tools/technologies on the job.

        Import and Export raw data

        Contribute to Mapping specifications

        Utilize SAS/R programming/Python programming skills for clinical trial study submissions

        Develop programs identifying data issues and reporting them to the appropriate team

        Utilize appropriate guidelines to build CDISC/regulatory compliant datasets

        Understand CRF annotations and check for consistency with raw data

        Ability to debug custom functions/SAS Macros and fix issues

        Good understanding of clinical data and domain

        Follow Client Processes and SOPs

        Assist senior team members in quality control processes

        Assist senior team members with team metrics

        Communicate with an internal team to create deliverables for pharmaceutical and CRO clients

        Work in tandem with Biostatistics and Data Management members on clinical projects

        Communicate with programming and statistics leads

        Make sure you are compliant with company policies/SOPs.

About US: Saama automates key clinical development and commercialization processes, with artificial intelligence (AI), Generative AI and advanced-analytics, accelerating your time to market. We offer AI-backed SaaS solutions as well as product-based industry services and accelerators. Discover more at saama.com.

 

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