Clinical SAS Programmer - Katalyst Healthcares & Life Sciences
Carlsbad, CA 92008
About the Job
Responsibilities:
- Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data.
- Generate SDTM domains, ADaM datasets, and Define.xml files .
- Assists in creation of table mock-ups under supervision of statisticians.
- Reviews output across programs to ensure consistency. Recognizes inconsistencies and initiates resolution of data problems.
- Typically creates programs using statistical analysis system language to support the clinical area.
- Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures.
- Implements data management plans designed to meet project and protocol deadline.
- Provides expertise in the design and development of clinical trials, protocols and case report forms.
- Acts as a liaison between clinical management, subcommittees and project teams as needed.
- Performs other duties as assigned
- BS/BA degree in Statistics, Mathematics, or Computer Science or in a related field and 2+ years of Biotechnology/Pharmaceutical/CRO industry experience as a clinical trial SAS Programmer programming CDISC data structures OR.
- Master's degree in Statistics, Mathematics, or Computer Science or in a related field and Some experience noted above.
- Understands Neurocrine's business objectives and developing understanding of Neurocrine's services and customers.
- Has experience in specific functional discipline while working to acquire higher-level knowledge and skills.
- Good project management skills.
- Knowledge of Biotechnology/Pharmaceutical/CRO industry, specifically clinical trial SAS programming, CDISC data structures.
- Strong knowledge of statistical programming tools such as STAT, R, SAS.
- Demonstrates knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines.
Source : Katalyst Healthcares & Life Sciences