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Senior Statistical Programmer

10+ years
₹20 LPA – ₹30 LPA
10 July 22, 2025
Job Description
Job Type: Full Time Education: BCS/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Statistical Programmer
Location: [Not specified]
Experience Required: 10+ years in clinical reporting/statistical programming
Job Type: Full-Time


Job Description:
We are currently seeking a Senior Statistical Programmer (SR SPA I) to join our growing team. This independent role involves supporting the clinical reporting production programming and verification for client regulatory submissions and publications. You will be primarily responsible for SDTM/ADaM dataset development, statistical and clinical reporting, and submissions support aligned with regulatory requirements.


Key Responsibilities:

Statistical Programming & Analysis:

  • Independently perform SAS programming and analysis to support the creation of analysis datasets, listings, figures, and tables.

  • Develop SAS application code for reporting needs and submission packages.

  • Conduct validation of SAS programs and deliverables to ensure accuracy and compliance.

CDISC Mapping & Deliverables:

  • Map and generate SDTM and ADaM datasets based on sponsor-specific or CDISC standards.

  • Deliver statistical appendices required for Clinical Trial Reports (CTR), Integrated Summary of Safety (ISS), and Integrated Summary of Efficacy (ISE).

  • Prepare data files and outputs for safety updates, scientific publications, and conference presentations.

Technical Expertise:

  • Perform migrations, verifications, and troubleshoot technical issues across platforms.

  • Participate as an expert in define.xml generation, SCE, PK/PD data processing, graphical outputs, and registry data support.

Collaboration & Consultation:

  • Collaborate with cross-functional client teams and internal stakeholders at DataCeutics.

  • Serve as a domain expert in areas such as SDTM, ADaM, SAS-based programming, or project coordination.


Desirable Skills and Experience:

  • 10+ years of experience in the pharmaceutical or CRO industry.

  • Strong programming expertise in SAS/Base, SAS/Macro, and SAS/STAT.

  • Proven proficiency in CDISC standards, SDTM, and ADaM.

  • Experience across multiple platforms (e.g., Windows, UNIX) is desirable.

  • Solid foundation in statistics/statistical analysis.

  • Ability to work independently with minimal supervision.

  • Exceptional attention to detail and documentation practices.


Estimated Salary: ₹20 LPA – ₹30 LPA (based on experience and skillset)