Description

Develop and maintain SAS programs to process clinical trial data according to protocol and statistical analysis requirements.

This role is on-site.

Responsibilities

• Create ADaM datasets from SDTM and raw datasets following CDISC analysis data model standards.
• Write, test, run, document, and QC SAS programs and macros to generate datasets, spreadsheets, listings, tables, and graphical displays.
• Develop standard programs and macros to convert raw datasets into standard formats and drive continuous improvement.
• Collaborate with managers and other programmers through formal and ad-hoc meetings.

Required Skills

• 4+ years of experience in statistical programming or related clinical data roles.
• Proficiency in SAS programming languages.
• Hands-on experience with CDISC standards.
• Experience performing QC on SAS programs and macros.
• Ability to interpret clinical trial objectives, designs, endpoints, and procedures defined in protocols.
• Bachelor's degree in Computer Science, Statistics, Engineering, or a related field.

Key Skills

Education

Bachelor's Degree