Description

Lead clinical study planning, data standardization, and SAS programming for clinical datasets.

This role is on-site.

Responsibilities

• Design clinical study databases and resolve discrepancy queries.
• Create SDTM Domain specifications and Define.xml documentation.
• Map raw data to SDTM standards and SDTM to ADaM domains.
• Develop SAS macros to automate variable mapping, view generation, and reporting.
• Build conversion, loading, and merging programs to transfer non-CRF data into OC databases.

Required Skills

• Expertise in SAS programming: SAS/BASE, SAS/STAT, SAS MACROS, SAS/ACCESS, SAS/GRAPH.
• Proficiency in PL/SQL.
• Experience with UNIX environments.
• Ability to generate HTML output using SAS/ODS.
• Knowledge of Object Oriented Programming.
• Experience mapping data from OC views and extracting raw datasets.
• Ability to review CRFs to ensure data collection consistency with protocol objectives.

Preferred Skills

• Experience with clinical study design and data definition standards.

Key Skills

Education

Any graduate