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Manager 1, Statistical Programming

Sun Pharma
8+ years
INR 30-45 LPA
Remote
10 June 16, 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, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Key Responsibilities

Clinical Programming Leadership

  • Lead statistical programming activities across multiple clinical studies and projects.

  • Ensure timely delivery of high-quality programming outputs.

  • Manage therapeutic area or compound/indication-specific programming activities.

CDISC & Dataset Development

  • Develop and maintain programming documentation.

  • Create and review:

    • SDTM Mapping Specifications

    • ADaM Specifications

  • Ensure compliance with CDISC standards.

SAS Programming

  • Develop and validate SAS programs for:

    • SDTM datasets

    • ADaM datasets

    • Tables, Listings, and Figures (TLFs)

  • Support analysis and reporting activities.

Regulatory Submission Support

  • Prepare and manage:

    • aCRF

    • define.xml

    • cSDRG

    • ADRG

    • ARM

  • Support submissions to:

    • FDA

    • EMA

    • PMDA

    • Other global regulatory agencies

Standards & Process Improvement

  • Contribute to:

    • Programming standards

    • SOPs

    • Standard macros

    • Best practices

  • Act as a Subject Matter Expert (SME) on programming topics.

Cross-Functional Collaboration

  • Work closely with:

    • Biostatistics

    • Data Management

    • Clinical Operations

    • Regulatory Affairs

    • External vendors

Review Activities

  • Participate in:

    • CRF annotation

    • SAP review

    • TLF specification review

    • Quality review activities

People Development

  • Mentor and coach junior programmers.

  • Support onboarding and training initiatives.


Required Skills

Technical Skills

  • Advanced SAS Programming

  • CDISC (SDTM, ADaM)

  • Regulatory Submission Standards

  • Clinical Trial Data Processing

  • Knowledge of:

    • R (preferred)

    • Python (preferred)

Domain Knowledge

  • Clinical Development Processes

  • Statistical Concepts & Methodologies

  • NDA/ANDA Regulatory Submissions

  • TAUG and Regulatory Guidelines

Soft Skills

  • Leadership

  • Problem Solving

  • Communication

  • Stakeholder Management

  • Team Collaboration

  • Project Planning


Seniority Level

People Manager / Lead Statistical Programmer


Experience Required

  • 8+ years of Statistical Programming experience

  • Experience in Biotechnology, Pharmaceutical, CRO, or Healthcare industries


Educational Qualification

  • Bachelor's degree in:

    • Statistics

    • Computer Science

    • Mathematics

    • Engineering

    • Life Sciences

    • Related disciplines