Read more

CHANDRAWAR IT TECHNOLOGIES PVT LTD; Sale; On-site; GBP 35,000 - 60,000; Full time

Job summary

CHANDRAWAR IT TECHNOLOGIES PVT LTD is seeking a skilled SAS programmer to support clinical trial data programming and reporting in a regulated environment. The role focuses on developing, validating, and maintaining SAS programs, creating TLFs, and contributing to CDISC-compliant SDTM/ADaM datasets; collaboration with biostatisticians and data managers is essential.

The position requires attention to data quality, reproducibility and documentation, with opportunities to contribute to study

Responsibilities

• Develop, maintain and validate SAS programs for clinical trial data.
• Create and validate analysis datasets, tables, listings and figures (TLFs).
• Support the development of SDTM and ADaM datasets in accordance with CDISC standards.
• Perform statistical programming for safety and efficacy analyses.
• Review programming specifications and statistical analysis plans.
• Perform quality control checks and investigate discrepancies.
• Develop and maintain SAS macros and reusable programming utilities.
• Ensure programming outputs are accurate, reproducible and properly documented.
• Support data review and reconciliation activities.
• Collaborate with biostatisticians, data managers and clinical project teams.
• Contribute to clinical study reports and regulatory submission deliverables where required.
• Follow company standard operating procedures, programming standards and quality processes.

Skills

SAS programming

SAS macros

CDISC standards

Quality control

Tools

SAS

SAS Macros

CDISC SDTM/ADaM

Job description

Develop, maintain and validate SAS programs for clinical trial data.

Create and validate analysis datasets, tables, listings and figures (TLFs).

Support the development of SDTM and ADaM datasets in accordance with CDISC standards.

Perform statistical programming for safety and efficacy analyses.

Review programming specifications and statistical analysis plans.

Perform quality control checks and investigate discrepancies.

Develop and maintain SAS macros and reusable programming utilities.

Ensure programming outputs are accurate, reproducible and properly documented.

Support data review and reconciliation activities.

Collaborate with biostatisticians, data managers and clinical project teams.

Contribute to clinical study reports and regulatory submission deliverables where required.

Follow company standard operating procedures, programming standards and quality processes.