Clinical SAS Programmer

Responsibilities :

• Effectively designs and codes SAS programs using BASE / SAS, SAS / STAT, SAS / GRAPH and SAS MACROS for assigned clinical projects(s).
• Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets.
• Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements.
• Provides input in the design and development of case report forms and clinical databases.
• Performs quality control checks / validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs.
• Programs quality checks for clinical study raw data and report the findings to Data Management.
• Provides input in the design and development of case report forms and clinical study databases.
• Reviews or author eCRF, SDTM and ADaM datasets specifications for datasets programming.
• Provides programming support for adhoc analysis.
• Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications).
• Manages timelines and schedules of specific phases of projects with internal personnel and external vendors.
• Acts as lead programmer for a study.
• Reviews or validates statistical deliverables of vendors for assigned project(s).

Requirements :