Found Description
Job title : Principal Statistical Programmer
Reports to : VP Operations
Job Purpose :
To lead the programming, validation, and delivery of high-quality statistical outputs for clinical trials by applying advanced SAS programming and CDISC standards, ensuring data integrity, regulatory compliance, and timely support of statistical analyses, clinical study reports, and regulatory submissions through close collaboration with biostatistics, data management, and clinical teams.
Duties and responsibilities :
Programming & Data Management :
Develop and maintain SAS programs for clinical trial data processing, analysis, and reporting.
Map clinical trial data to CDISC standards (SDTM and ADa M) ensuring compliance with regulatory requirements.
Create and maintain analysis datasets following CDISC implementation guidelines.
Perform data validation and quality control checks to ensure data integrity.
Expertise as Clinical SAS programmer: SAS programming language and ...
Reports to : VP Operations
Job Purpose :
To lead the programming, validation, and delivery of high-quality statistical outputs for clinical trials by applying advanced SAS programming and CDISC standards, ensuring data integrity, regulatory compliance, and timely support of statistical analyses, clinical study reports, and regulatory submissions through close collaboration with biostatistics, data management, and clinical teams.
Duties and responsibilities :
Programming & Data Management :
Develop and maintain SAS programs for clinical trial data processing, analysis, and reporting.
Map clinical trial data to CDISC standards (SDTM and ADa M) ensuring compliance with regulatory requirements.
Create and maintain analysis datasets following CDISC implementation guidelines.
Perform data validation and quality control checks to ensure data integrity.
Expertise as Clinical SAS programmer: SAS programming language and ...
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