Senior /Principal Statistical Programmer

Avance Clinical Pty; India; Hybrid; INR 2,000,000 - 3,200,000; Full time

Job summary

Avance Clinical Pty in Bengaluru is seeking a Senior/Principal Statistical Programmer to develop, validate, and maintain statistical programming outputs for clinical trials. You will collaborate with biostatisticians and data management to ensure regulatory compliance.

Responsibilities include preparing listings, tables and figures for study reports, creating primary and QC SAS programs for CDISC datasets, and assisting with analysis plans and randomization schedules while maintaining CDISC

Qualifications

• Ordinary degree in the appropriate discipline or equivalent industry experience.
• Minimum 8 years’ experience in statistical programming in pharmaceutical/health research.
• Minimum 2–3 years in Oncology Therapeutics Area Programming.
• Strong CDISC knowledge and SDTM conversion experience.
• Experience with development, documentation, and testing of analysis data and programming code to meet regulatory standards.

Responsibilities

• Develop, validate, and maintain statistical programming outputs for clinical trials.
• Prepare listings, tables and figures for study reports.
• Create primary and QC SAS programs for CDISC datasets and documentation.
• Assist with statistical analysis plans and randomization schedules.
• Coordinate with Data Management and labs on data transfer.
• Maintain CDISC standards and contribute to process improvements.

Skills

CDISC SDTM knowledge

SAS programming

Oncology programming

Regulatory compliance

Education

Bachelor's degree in life sciences or biostatistics

Tools

SAS

CDISC standards

Job description

Senior /Principal Statistical Programmer

Join our expanding team in India, office based in Bangalore!

16th October, 2026

Who are we?

We’reAvance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this areawith our founding roots dating back to the 1980’s. If youalreadywork in thisindustryyou’llknow that we are experts in our field.

Why should you join Avance Clinical?

We appreciate that our most important asset is our people. We offer a fun, friendly workenvironmentand a culture that values honesty and respect.We havea strong senseof team. We genuinely appreciateeach individualbut recognise the collectivewhenachieving success. We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.

Broad Purpose

This is a full-time on-site/hybrid role for a Statistical Programmer based in Bengaluru. The Senior/Principal Statistical Programmer will be responsible for developing, validating, and maintaining statistical programming outputs including datasets, listings, tables, and graphs for clinical trials. This role involves collaborating with biostatisticians and data management teams, programming complex algorithms, writing macros, managing datasets, and ensuring compliance with regulatory requirements.

• Preparation of listings, tables and figures for clinical study reports.
• Creation of primary and QC SAS programs for CDISC datasets and associated documentation.
• Assists with the preparation of statistical analysis plans (including preparation/review of listing, table and figure shells) and randomization schedules.
• Liaising with Data Management team and bioanalytical laboratories regarding data transfer.
• Management of project specific programming tasks and deliverables (including maintenance of planning documents and regular communication with internal stakeholders) to ensure project team will provide statistical programming deliverables according to project timelines.
• Maintain and coordinate CDISC standards, ensure maximum reuse of applied standards and involvement in ongoing process improvement initiatives
• Stay current with the evolution of all CDISC standards and be involved in creation and maintenance of process documentation
• Contribute to the development and improvement of Avance procedures related to statistical programming.
• Other duties as directed by Line Management or delegate.

16th October, 2026

Who are we?

We’reAvance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this areawith our founding roots dating back to the 1980’s. If youalreadywork in thisindustryyou’llknow that we are experts in our field.

Why should you join Avance Clinical?

We appreciate that our most important asset is our people. We offer a fun, friendly workenvironmentand a culture that values honesty and respect.We havea strong senseof team. We genuinely appreciateeach individualbut recognise the collectivewhenachieving success. We are committed to creating a flexible work environment for our people by supporting them to balance their work commitments and personal needs, both now and into the future.

Broad Purpose

This is a full-time on-site/hybrid role for a Statistical Programmer based in Bengaluru. The Senior/Principal Statistical Programmer will be responsible for developing, validating, and maintaining statistical programming outputs including datasets, listings, tables, and graphs for clinical trials. This role involves collaborating with biostatisticians and data management teams, programming complex algorithms, writing macros, managing datasets, and ensuring compliance with regulatory requirements.

• Preparation of listings, tables and figures for clinical study reports.
• Creation of primary and QC SAS programs for CDISC datasets and associated documentation.
• Assists with the preparation of statistical analysis plans (including preparation/review of listing, table and figure shells) and randomization schedules.
• Liaising with Data Management team and bioanalytical laboratories regarding data transfer.
• Management of project specific programming tasks and deliverables (including maintenance of planning documents and regular communication with internal stakeholders) to ensure project team will provide statistical programming deliverables according to project timelines.
• Maintain and coordinate CDISC standards, ensure maximum reuse of applied standards and involvement in ongoing process improvement initiatives
• Stay current with the evolution of all CDISC standards and be involved in creation and maintenance of process documentation
• Contribute to the development and improvement of Avance procedures related to statistical programming.
• Other duties as directed by Line Management or delegate.

Qualifications, Skills and Experience

• Ordinary degree in the appropriate discipline or appropriate industry experience.
• Minimum 8 years’ experience in statistical programming in pharmaceutical / health research.
• Minimum 2-3 years in Oncology Therapeutics Area Programming
• Strong CDISC knowledge and SDTM conversion experience
• Experience with development, documentation, and testing of analysis data and programming code to meet regulatory and company standards