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The primary function of this position is to develop, implement, and maintain clinical database systems. Key responsibilities include extracting clinical data from clinical data management systems, producing standard and custom reports in SAS, and performing Study Data Tabulation Model (SDTM) conversion programming.
Key Responsibilities- Extract and manipulate large datasets using SQL and SAS programming languages.
- Develop and implement data transfer specifications with vendors for external data sources.
- Perform consistency checks on data transfers between internal and external parties to ensure completeness and accuracy.
- Convert raw clinical trial data into SDTM format for further analysis.
- Conduct Quality Control (QC) on programming work performed by fellow Database Programmers.
- Bachelor's degree or certification in Computer Science, Information Technology, or a related field.
- Minimum 5 years of experience in clinical SAS programming within the pharmaceutical industry.
- Working knowledge of CDISC SDTM mapping, specs, conversion, domains, datasets, eCRF/eCRT Package, and define.xml development.
- Understanding of regulatory requirements relevant to submissions.
- Knowledge of clinical trial study design and electronic data submission requirements.
- Strong communication and interpersonal skills, with the ability to collaborate effectively as part of a team.
Our organization values diversity and rewards high performance. In addition to a competitive salary, we provide a range of benefits focused on well-being and work-life balance opportunities for you and your family.
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