SrPrincipal Statistical Programmer
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Job Location:
Monthly Salary:
Posted on:
17 hours ago
Vacancies:
1 Vacancy
Job Summary
*** JOB DESCRIPTION ***
OVERVIEW
As the Senior Statistical Programmer you will work with the Principal Technical Consultant and provide SAS
programming expertise in data extraction from various databases TLG programming developing programming and
validation specifications. You will provide hands-on expertise in programming SDTM and ADaM datasets to
support various analyses and TLG Programming. You will be responsible for developing and
maintaining programming and validation specifications for TLGs as per requirements provided by the
Biostatistician.
As the Senior Statistical Programmer you will work with the Principal Technical Consultant and provide SAS
programming expertise in data extraction from various databases TLG programming developing programming and
validation specifications. You will provide hands-on expertise in programming SDTM and ADaM datasets to
support various analyses and TLG Programming. You will be responsible for developing and
maintaining programming and validation specifications for TLGs as per requirements provided by the
Biostatistician.
KEY TASKS & RESPONSIBILITIES
Create and maintain SAS programs to produce outputs to support the analysis and reporting of
clinical trials
Develop analysis datasets for trial level reporting and integrated safety and efficacy activities
Program and QC data listings summaries and graphs as defined in SAP. If required validate the
statistical models used for programming
Develop re-usable utility macros in order to build a macro library to support programming tables
listing and graphs for phase 1-4 clinical trial reporting
Collaborate with the project team to ensure the deliverables are completed on time with high quality
Create submission-ready standard data presentations and data sets using standard coding and
following standard industry processes including SDLC
Maintain all project documentation as required by SOP and Processes
Ensure compliance with eClinical Solutions and industry quality standards guidelines and
procedures
Other duties as assigned
clinical trials
Develop analysis datasets for trial level reporting and integrated safety and efficacy activities
Program and QC data listings summaries and graphs as defined in SAP. If required validate the
statistical models used for programming
Develop re-usable utility macros in order to build a macro library to support programming tables
listing and graphs for phase 1-4 clinical trial reporting
Collaborate with the project team to ensure the deliverables are completed on time with high quality
Create submission-ready standard data presentations and data sets using standard coding and
following standard industry processes including SDLC
Maintain all project documentation as required by SOP and Processes
Ensure compliance with eClinical Solutions and industry quality standards guidelines and
procedures
Other duties as assigned
Key Skills
- Business Development
- Customer Service
- Attorney
- CISSP
- Data Analysis
