Statistical Programmer

Saama; Pune District; On-site; INR 700,000 - 1,000,000; Full time

Job summary

Saama is seeking a Statistics Programmer – L2 in Pune to independently handle SDTM mappings and client-specific mappings for standard domains. The role requires analytic understanding of clinical data, mapping logic, and data issue resolution within our AI-enabled SaaS environment.

Ideal candidates have 2–4 years of experience, knowledge of CDISC standards, SAS programming, and familiarity with Python or R.

Qualifications

• 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.

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.

Skills

Clinical Domain knowledge

CDISC Standards

SAS Programming

Python Programming

R Programming

Communication & teamwork

Education

Graduation in Pharmacy/Computer Science

Job description

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.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.

Description

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.