Statistical Programmer - Katalyst CRO : Job Details

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• The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
• The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.
• Develop and validate SAS programs to support clinical trial data analysis and reporting.
• Create, maintain, and document SAS programming standards and procedures.
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.
• Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.
• The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.
• Prepare datasets for analysis, including merging and cleaning data from various sources.
• Prepare and review tables, listings, and figures for clinical study reports.
• Ensure compliance with regulatory requirements and guidelines.
• Keep up to date with new SAS programming methods and software, as well as regulatory guidance.

Responsibilities

• The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
• The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting.
• Develop and validate SAS programs to support clinical trial data analysis and reporting.
• Create, maintain, and document SAS programming standards and procedures.
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met.
• Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency.
• The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry.
• Prepare datasets for analysis, including merging and cleaning data from various sources.
• Prepare and review tables, listings, and figures for clinical study reports.
• Ensure compliance with regulatory requirements and guidelines.
• Keep up to date with new SAS programming methods and software, as well as regulatory guidance.

Requirements:

• Bachelor's Degree in statistics, computer science, or a similar quantitative field.
• 4+ years of clinical statistical programming experience within the pharmaceutical or related industry.
• Proficiency in SAS programming.
• Knowledge of CDISC data standards.
• Strong attention to detail and ability to work independently.
• Excellent problem-solving skills.
• Excellent verbal and written communication skills.
• Knowledge of regulatory requirements for clinical trials and drug development.
• Ability to work in a team environment and collaborate effectively with other stakeholders.

Seniority level

• Seniority levelAssociate

Employment type

• Employment typeContract

Job function

• Job functionInformation Technology
• IndustriesPharmaceutical Manufacturing

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