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Statistical Programmer Ii

AstraZeneca
2-5 years
INR 10 LPA – 18 LPA
PAN-India, India
1 June 15, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. 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

Statistical Programmer II

Location: India
Company: AstraZeneca
Employment Type: Full-Time

Job Summary

The Statistical Programmer II is responsible for developing, validating, and maintaining clinical trial datasets and statistical outputs that support clinical development, regulatory submissions, and decision-making. This role involves programming SDTM and ADaM datasets, generating Tables, Listings, and Figures (TLFs), ensuring compliance with CDISC standards, and collaborating with cross-functional study teams to deliver high-quality, regulatory-compliant statistical programming solutions.


Key Responsibilities

Clinical Data Standards Programming

  • Develop and validate SDTM and ADaM datasets for clinical studies.

  • Ensure traceability, consistency, and compliance with CDISC implementation standards.

  • Support data transformations, derivations, and dataset creation activities.

  • Maintain programming documentation and dataset specifications.

Statistical Analysis & Reporting

  • Program, validate, and generate Tables, Listings, and Figures (TLFs) according to Statistical Analysis Plans (SAPs).

  • Support clinical study reporting and regulatory submission deliverables.

  • Ensure statistical outputs are accurate, reproducible, and audit-ready.

  • Document programming methodologies and validation processes.

Quality & Regulatory Compliance

  • Adhere to established programming standards, SOPs, and regulatory guidelines.

  • Perform quality control and validation of programming deliverables.

  • Ensure compliance with industry standards including CDISC SDTM and ADaM.

  • Support inspection readiness and regulatory submission requirements.

Protocol & Study Support

  • Interpret clinical study protocols and statistical analysis plans.

  • Understand study objectives and translate them into programming solutions.

  • Anticipate data requirements and proactively address programming challenges.

  • Support clinical development activities through data-driven insights.

Cross-Functional Collaboration

  • Collaborate with statisticians, data managers, clinical scientists, and lead programmers.

  • Communicate project progress, risks, and timelines effectively.

  • Participate in study team meetings and technical discussions.

  • Support end-to-end clinical trial delivery through effective teamwork.

Technical Development & Innovation

  • Expand expertise in SAS programming and clinical data standards.

  • Utilize R or Python for exploratory analysis, automation, and data quality checks where applicable.

  • Contribute to process improvement initiatives and programming efficiencies.

  • Stay updated on industry trends, emerging technologies, and regulatory requirements.


Required Qualifications

Education

  • Bachelor's or Master's degree in Statistics, Mathematics, Biostatistics, Computer Science, Engineering, Life Sciences, Pharmacy, or a related discipline.

Experience

  • 2–5 years of experience in Statistical Programming, Clinical Data Analysis, or Biostatistics.

  • Experience supporting clinical trials within pharmaceutical, biotechnology, or CRO environments.

  • Hands-on experience with SDTM, ADaM, and TLF development.