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Senior Executive, Statistical Programming

Sun Pharma
2+ years
INR 6-10LPA
Gurgaon, India
10 June 17, 2026
Job Description
Job Type: Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Key Responsibilities

Clinical Trial Programming

  • Support statistical programming activities across Phase I-IV clinical studies.

  • Deliver programming outputs according to study timelines and quality standards.

  • Collaborate with study teams and programming leads.

CDISC Implementation

  • Develop and maintain SDTM mapping specifications.

  • Create ADaM specifications and datasets.

  • Ensure compliance with CDISC standards and regulatory requirements.

Statistical Programming

  • Develop SAS programs for:

    • SDTM datasets

    • ADaM datasets

    • Tables

    • Listings

    • Figures (TLFs)

  • Validate programming outputs for quality and accuracy.

Regulatory Submission Support

  • Prepare and support:

    • Define.xml

    • aCRF

    • cSDRG

    • ADRG

    • ARM

  • Support submissions to:

    • FDA

    • EMA

    • PMDA

    • Other global health authorities

Documentation & Standards

  • Maintain programming documentation.

  • Participate in development of utility and standard macros.

  • Support programming standards implementation.

Study Support Activities

  • Participate in:

    • CRF Annotation

    • TLF Specification Development

    • Macro Development

    • Post-hoc Analysis

    • Ad-hoc Reporting


Required Skills

Technical Skills

  • SAS Programming

  • SDTM Development

  • ADaM Development

  • CDISC Standards

  • TLF Programming

  • Clinical Trial Data Analysis

  • Define.xml Generation

  • Regulatory Submission Packages

Regulatory Knowledge

  • FDA Submission Requirements

  • EMA Guidelines

  • PMDA Guidelines

  • eCTD Standards

  • SDTM Implementation Guide

  • TAUG

  • Data Submission Compliance

Programming Skills

Mandatory

  • SAS Base

  • SAS Macro Programming

  • SAS SQL

Preferred

  • R Programming

  • Python


Soft Skills

  • Analytical Thinking

  • Problem Solving

  • Communication Skills

  • Team Collaboration

  • Time Management

  • Attention to Detail

  • Adaptability

  • Ownership & Accountability


Preferred Knowledge

  • Clinical Trial Design

  • Biostatistics Concepts

  • Regulatory Submission Processes

  • NDA/ANDA Submissions

  • Pharmaceutical Drug Development Lifecycle

  • End-to-End Statistical Programming