Clinical SAS Programmer

Responsibilities :

• Attending multi-disciplinary team meetings, representing the programming function.
• Create or review and approve programming plans at study and project level.
• Provide input on key study-related documents produced by other functions ( CRFs, Data Management Plan, SAPs, etc.)
• Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
• Develop software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
• Assist statisticians by suggesting algorithms to address Client analysis requests.
• Develop software validation procedures and test plans, as necessary.
• Create and document archives of software, outputs, and analysis files.
• Create and maintain department SOPs related to clinical programming.

Requirements :