Statistical Programmer

Responsibilities :

• Demonstrated practical understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry.
• Demonstrated satisfactory ability to apply SAS programming knowledge and work independently to solve problems related to non-routine situations.
• Responsible for the creation and validation of SDTM, ADaM and TLFs for CSR, ISS, and Client following SOPs, department, and project standards.
• Ensure internal consistency of output and assess consistency with other activities for the project (e.g., ISS, Client), as applicable.
• Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and resolving Pinnacle21 checks.
• Responsible for the creation and accuracy of derivations as defined in the protocol and statistical analysis plan.
• Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications.
• Ensure consistency across studies within a project.
• Responsible for the creationof data definition documents, TOCs, and support submission related activities.
• Learn and maintain expertisein the use of the utilities and macros developed for the Statistical Programmers.
• Develop new macros and utilities.
• Provide accurateand timely responses to requests from clients with a sense of urgency.
• Be compliant with training requirements.

Requirements :