Clinical SAS Programmer SAS And R Programming

2COMS Consulting Pvt. Ltd.; Hyderabad; Remote; INR 900,000 - 1,500,000; Full time

Benefits offered by this job

Work From Home

Job summary

2COMS Consulting Pvt. Ltd. is seeking a Clinical SAS Programmer with hands-on SAS and R programming to support clinical trial data analysis and regulatory submissions.

ThisPermanent Work From Home role is Pan India, requiring 3+ years in SAS, 1+ year in R, and SDTM/ADaM expertise; certification is mandatory, with a 30–60 day notice period.

Qualifications

• 3+ years of experience in Clinical SAS Programming.
• At least 1 year hands-on R Programming experience.
• Strong knowledge of SDTM and ADaM standards.
• Experience in developing and validating clinical trial datasets.
• Experience with Tables, Listings, and Figures (TLFs).
• SAS macros, data manipulation, statistical programming, and quality control.
• Certification in Clinical SAS Programming is required.
• Strong analytical, problem-solving, and communication skills.

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.

Skills

Clinical SAS Programming

R Programming

SDTM/ADaM

TLFs

SAS Macros

Data Manipulation

Quality Control

Statistical Programming

Education

Clinical SAS Programming Certification

Job description

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

Requirements: