Verified Job
IT / Software / Data Analyst
SAS Programmer
IT / Software / Data Analyst
#714260
Remote / WFH
Job Description
Role Overview:
You will be a SAS Programmer working full-time in a remote capacity. Your main responsibilities will include developing, testing, and maintaining SAS programs to facilitate data analysis for clinical trials. This will involve tasks such as creating datasets, producing tables/listings/figures, collaborating with various teams, and ensuring adherence to regulatory standards. Additionally, you will be tasked with troubleshooting technical issues and streamlining programming processes for improved accuracy and efficiency.
Key Responsibilities:
- Develop, test, and maintain SAS programs to support data analysis for clinical trials
- Create datasets and generate tables/listings/figures
- Collaborate with cross-functional teams to ensure project success
- Ensure compliance with regulatory standards, including CDISC (SDTM/ADaM)
- Troubleshoot technical challenges and optimize programming workflows
- Work on data management and reporting tasks related to clinical trial data analysis
- Interpret and apply industry guidelines effectively
- Collaborate with data managers and statisticians
- Maintain databases and oversee quality control processes
Qualification Required:
- Proficiency in SAS programming, with expertise in data management and reporting
- Experience in clinical trial data analysis, statistical programming, and interpretation
- Knowledge of regulatory standards and industry guidelines, including CDISC (SDTM/ADaM)
- Ability to work effectively in multidisciplinary teams
- Strong problem-solving skills and attention to detail in managing databases and quality control
- Educational background in Statistics, Computer Science, Data Science, or related field
- Familiarity with R Programming and data visualization tools is a plus
- Effective written and verbal communication skills with remote timeline management capabilities
(Note: Additional details about the company were not provided in the job description.) Role Overview:
You will be a SAS Programmer working full-time in a remote capacity. Your main responsibilities will include developing, testing, and maintaining SAS programs to facilitate data analysis for clinical trials. This will involve tasks such as creating datasets, producing tables/listings/figures, collaborating with various teams, and ensuring adherence to regulatory standards. Additionally, you will be tasked with troubleshooting technical issues and streamlining programming processes for improved accuracy and efficiency.
Key Responsibilities:
- Develop, test, and maintain SAS programs to support data analysis for clinical trials
- Create datasets and generate tables/listings/figures
- Collaborate with cross-functional teams to ensure project success
- Ensure compliance with regulatory standards, including CDISC (SDTM/ADaM)
- Troubleshoot technical challenges and optimize programming workflows
- Work on data management and reporting tasks related to clinical trial data analysis
- Interpret and apply industry guidelines effectively
- Collaborate with data managers and statisticians
- Maintain databases and oversee quality control processes
Qualification Required:
- Proficiency in SAS programming, with expertise in data management and reporting
- Experience in clinical trial data analysis, statistical programming, and interpretation
- Knowledge of regulatory standards and industry guidelines, including CDISC (SDTM/ADaM)
- Ability to work effectively in multidisciplinary teams
- Strong problem-solving skills and attention to detail in managing databases and quality control
- Educational background in Statistics, Computer Science, Data Science, or related field
- Familiarity with R Programming and data visualization tools is a plus
- Effective written and verbal communication skills with remote timeline management capabilities
(Note: Additional details about the company were not provided in the job description.)
You will be a SAS Programmer working full-time in a remote capacity. Your main responsibilities will include developing, testing, and maintaining SAS programs to facilitate data analysis for clinical trials. This will involve tasks such as creating datasets, producing tables/listings/figures, collaborating with various teams, and ensuring adherence to regulatory standards. Additionally, you will be tasked with troubleshooting technical issues and streamlining programming processes for improved accuracy and efficiency.
Key Responsibilities:
- Develop, test, and maintain SAS programs to support data analysis for clinical trials
- Create datasets and generate tables/listings/figures
- Collaborate with cross-functional teams to ensure project success
- Ensure compliance with regulatory standards, including CDISC (SDTM/ADaM)
- Troubleshoot technical challenges and optimize programming workflows
- Work on data management and reporting tasks related to clinical trial data analysis
- Interpret and apply industry guidelines effectively
- Collaborate with data managers and statisticians
- Maintain databases and oversee quality control processes
Qualification Required:
- Proficiency in SAS programming, with expertise in data management and reporting
- Experience in clinical trial data analysis, statistical programming, and interpretation
- Knowledge of regulatory standards and industry guidelines, including CDISC (SDTM/ADaM)
- Ability to work effectively in multidisciplinary teams
- Strong problem-solving skills and attention to detail in managing databases and quality control
- Educational background in Statistics, Computer Science, Data Science, or related field
- Familiarity with R Programming and data visualization tools is a plus
- Effective written and verbal communication skills with remote timeline management capabilities
(Note: Additional details about the company were not provided in the job description.) Role Overview:
You will be a SAS Programmer working full-time in a remote capacity. Your main responsibilities will include developing, testing, and maintaining SAS programs to facilitate data analysis for clinical trials. This will involve tasks such as creating datasets, producing tables/listings/figures, collaborating with various teams, and ensuring adherence to regulatory standards. Additionally, you will be tasked with troubleshooting technical issues and streamlining programming processes for improved accuracy and efficiency.
Key Responsibilities:
- Develop, test, and maintain SAS programs to support data analysis for clinical trials
- Create datasets and generate tables/listings/figures
- Collaborate with cross-functional teams to ensure project success
- Ensure compliance with regulatory standards, including CDISC (SDTM/ADaM)
- Troubleshoot technical challenges and optimize programming workflows
- Work on data management and reporting tasks related to clinical trial data analysis
- Interpret and apply industry guidelines effectively
- Collaborate with data managers and statisticians
- Maintain databases and oversee quality control processes
Qualification Required:
- Proficiency in SAS programming, with expertise in data management and reporting
- Experience in clinical trial data analysis, statistical programming, and interpretation
- Knowledge of regulatory standards and industry guidelines, including CDISC (SDTM/ADaM)
- Ability to work effectively in multidisciplinary teams
- Strong problem-solving skills and attention to detail in managing databases and quality control
- Educational background in Statistics, Computer Science, Data Science, or related field
- Familiarity with R Programming and data visualization tools is a plus
- Effective written and verbal communication skills with remote timeline management capabilities
(Note: Additional details about the company were not provided in the job description.)
