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Manager 2, Statistical Programming

Sun Pharma
4+ years
INR 18-12 LPA
Gurgaon, Remote, India
10 June 17, 2026
Job Description
Job Type: Hybrid 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

1. Study Leadership & Project Management

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

  • Manage multiple studies/projects within therapeutic areas or compounds.

  • Ensure timely delivery of high-quality programming outputs.

  • Coordinate with cross-functional teams and stakeholders.


2. CDISC Standards Implementation

  • Create and maintain:

    • SDTM Mapping Specifications

    • ADaM Specifications

  • Ensure compliance with:

    • CDISC Standards

    • Regulatory Guidelines

    • TAUG Requirements


3. Statistical Programming

Develop and review SAS programs for:

  • SDTM Dataset Creation

  • ADaM Dataset Creation

  • Tables

  • Listings

  • Figures (TLFs)

Ensure quality, efficiency, and compliance with study requirements.


4. Regulatory Submission Support

Handle regulatory submission deliverables including:

  • Define.xml

  • Annotated CRF (aCRF)

  • cSDRG

  • ADRG

  • ARM

  • eCRT Packages

Support submissions to:

  • FDA

  • EMA

  • PMDA

  • Other Global Health Authorities


5. Documentation & Compliance

  • Maintain programming documentation.

  • Ensure compliance with:

    • P21 Validation Checks

    • eCTD Guidelines

    • Regulatory Standards

    • Internal SOPs


6. Process Improvement

  • Develop standard SAS macros and utility programs.

  • Contribute to programming standards and best practices.

  • Participate in process optimization initiatives.


7. Review Activities

Participate in:

  • CRF Annotation Review

  • Statistical Analysis Plan (SAP) Review

  • TLF Specification Development

  • TLF Review Activities


8. Team Leadership & Mentoring

  • Mentor junior programmers.

  • Train and onboard new hires.

  • Act as Subject Matter Expert (SME).

  • Promote collaboration and knowledge sharing.


Required Technical Skills

Programming Skills

Mandatory

  • SAS Programming (Advanced)

Preferred

  • R Programming

  • Python Programming


Clinical & Regulatory Knowledge

Strong understanding of:

  • Clinical Trial Processes

  • Statistical Concepts

  • CDISC Standards

  • SDTM

  • ADaM

  • NDA Submissions

  • Regulatory Submission Requirements


Soft Skills

  • Strong Analytical Skills

  • Problem Solving Ability

  • Attention to Detail

  • Communication Skills

  • Team Collaboration

  • Time Management

  • Leadership Capability


Preferred Certifications

  • SAS Certified Base Programmer

  • SAS Certified Advanced Programmer

  • CDISC-related Certifications (preferred)