Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Biostatistical Programmer

Premier Research
6-8 years
Not Disclosed
India
10 March 20, 2026
Job Description
Job Type: Full Time Remote Education: B.Com/ BBA/ MBA/ M.Com/ B.Sc/ M.Sc/ B.Tech/ M.Tech/ BE/ ME and All Graduats Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Biostatistical Programmer | Remote | Premier Research

Company: Premier Research
Location: India (Remote)
Job Type: Full-Time
Experience: 6–8 Years
Qualification: Bachelor’s in Statistics / IT / Mathematics or related field


Job Overview

This is a senior-level role focused on SAS programming and clinical trial data analysis. You will work on SDTM datasets, develop statistical outputs, and collaborate with biostatistics and data management teams to support regulatory submissions.


Key Responsibilities

SAS Programming

  • Develop SAS programs for tables, listings, and figures (TLFs)

  • Generate CDISC-compliant datasets (SDTM/ADaM)

  • Create and validate SAS macros

Data & Analysis

  • Prepare dataset specifications

  • Support clinical trial data analysis and reporting

  • Assist Data Management with programming requirements

Quality Control

  • Perform code review, double programming, and log checks

  • Ensure accuracy and compliance of outputs

Collaboration

  • Work with biostatisticians and study teams

  • Act as Lead Programmer for assigned studies


Required Skills

  • Strong expertise in SAS programming

  • In-depth knowledge of CDISC standards (SDTM)

  • Understanding of clinical trial data and workflows

  • Knowledge of ICH and regulatory guidelines

  • Advanced macro programming and data handling


Eligibility Criteria

  • Bachelor’s degree in relevant field

  • 6–8 years of SAS programming experience in clinical trials

  • Experience with CDISC datasets and regulatory submissions


Why This Role

  • High-demand domain (Biostatistics + Programming)

  • Remote opportunity

  • Direct involvement in regulatory submissions

  • Strong career growth in clinical data science