Sr. SAS Programmer

Responsibilities :

• To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications.
• Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.
• Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas : SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g. Publications).
• ccessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files).
• Working with external vendors in order to develop or monitor the content and structure of SAS data sets.
• Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract / manuscripts) to ensure accuracy, quality, and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review.
• Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management.
• Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents.
• Maintaining standards for programming activities.
• Working independently to accomplish tasks and goals defined by supervisor.
• Bringing in new ideas to improve the programming process.

Requirements :