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Clinical SAS Programmer – SAS & R Programming

Role overview

Qualifications

  • Minimum 3+ years of experience in Clinical SAS Programming
  • At least 1 year of hands-on experience in R Programming
  • Strong knowledge of SDTM and ADaM standards
  • Relevant certification in Clinical SAS Programming

Responsibilities

  • Develop, maintain, and validate clinical trial datasets using SAS and R
  • Create and validate SDTM and ADaM datasets
  • Generate Tables, Listings, and Figures (TLFs) for clinical study reports
  • Ensure compliance with clinical research standards and regulatory requirements

Key facts

Hard skills

Other skills

  • Quality Control
  • Analytical Thinking
  • Problem Solving
  • Communication

About the company

2COMS Consulting Pvt. Ltd. logo

2COMS Consulting Pvt. Ltd.

Human Resources Services

2COMS Consulting focuses on the #HumanSideOfThings – helping organizations become sustainable leaders by connecting them to the right talent. We are a Human Supply Chain management company with over 10,515+ employees, spread across seven locations. As an NSDC partner, we help more than 4000 professionals meet their career goals by connecting them with over 70 clients, daily. Our manpower solutions are customized and aligned with our clients’ requirements – financial management, continuous performance improvement, and integrated technology enablement. It is our continuous endeavours of the past 20 years that helped us strengthen our relationships with our partners and gain diversified experience spanning industries. For more information, visit the link below: https://www.2coms.com/

Company details

IndustryHuman Resources Services
Company size10001

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Job description

Job Opening: Clinical SAS Programmer – SAS & R Programming

Experience: 3+ Years
Work Mode: Work From Home (WFH)
Location: Pan India
Notice Period: 30–60 Days

Job Description

We are looking for experienced Clinical SAS Programmers with hands-on expertise in Clinical SAS Programming and R Programming to support clinical trial data analysis, statistical programming, and regulatory submissions.

Mandatory Skills

  • Clinical SAS Programming – Mandatory

  • R Programming – Mandatory

  • Minimum 3+ years of relevant experience in SAS Programming.

  • At least 1 year of hands-on experience in R Programming is mandatory.

  • Strong knowledge of SDTM and ADaM standards.

  • Experience in developing and validating clinical trial datasets.

  • Knowledge of Tables, Listings, and Figures (TLFs).

  • SAS macros, data manipulation, statistical programming, and quality control.

  • Relevant Clinical SAS Programming certification is required.

Key Responsibilities

  • Develop, maintain, and validate clinical trial datasets using SAS and R.

  • Create and validate SDTM and ADaM datasets.

  • Generate Tables, Listings, and Figures (TLFs) for clinical study reports.

  • Perform programming validation, quality checks, and discrepancy resolution.

  • Ensure compliance with clinical research standards and regulatory requirements.

  • Maintain accurate programming documentation and collaborate with biostatistics and data management teams.

Candidate Requirements

  • Minimum 3+ years of experience in Clinical SAS Programming.

  • Minimum 1 year of hands-on R Programming experience is mandatory.

  • Practical experience with SDTM, ADaM, and clinical trial data.

  • Relevant certification in Clinical SAS Programming.

  • Strong analytical, problem-solving, and communication skills.

Important: Candidates with SAS experience but without at least 1 year of R Programming experience are not eligible for this requirement.

Work Arrangement: Permanent Work From Home | Pan India
Notice Period: 30–60 Days



Salary: 1200000- 2000000

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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