Medix™
We are looking for a Sr Statistical Programmer to support a biotech client of ours in Seattle, WA. Interested candidates must have 5+ years of experience in statistical programming for clinical research trials.
Details:
6+ month contract
Pay: $75hr OBO
Overview
The Senior Statistical Programmer provides advanced programming support and leads complex data analysis projects. This role develops and validates statistical programs, conducts quality control checks on data and analysis outputs, and optimizes programming processes and methodologies to ensure accuracy, efficiency, and compliance. Responsibilities
Develop and validate complex statistical programs. Conduct quality control checks on datasets and analysis outputs. Optimize programming processes and methodologies to improve efficiency. Lead complex data analysis projects, collaborating with statisticians and data managers to ensure accuracy. Document programming activities and maintain version control. Provide technical guidance and mentorship to junior programmers. Ensure compliance with regulatory requirements and industry standards. Troubleshoot and resolve programming issues. Required Qualifications
Bachelor’s degree in Statistics, Biostatistics, Computer Science, or a related field. 4+ years of experience in statistical programming. Proficiency in SAS, R, or Python. Preferred Qualifications
Experience in clinical trials or research studies. Knowledge of CDISC standards (SDTM, ADaM). Knowledge, Skills, and Abilities
Strong programming and problem-solving skills. Attention to detail and ability to perform rigorous quality checks. Effective communication and collaboration skills to work cross-functionally. Ability to lead projects and provide mentorship.
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The Senior Statistical Programmer provides advanced programming support and leads complex data analysis projects. This role develops and validates statistical programs, conducts quality control checks on data and analysis outputs, and optimizes programming processes and methodologies to ensure accuracy, efficiency, and compliance. Responsibilities
Develop and validate complex statistical programs. Conduct quality control checks on datasets and analysis outputs. Optimize programming processes and methodologies to improve efficiency. Lead complex data analysis projects, collaborating with statisticians and data managers to ensure accuracy. Document programming activities and maintain version control. Provide technical guidance and mentorship to junior programmers. Ensure compliance with regulatory requirements and industry standards. Troubleshoot and resolve programming issues. Required Qualifications
Bachelor’s degree in Statistics, Biostatistics, Computer Science, or a related field. 4+ years of experience in statistical programming. Proficiency in SAS, R, or Python. Preferred Qualifications
Experience in clinical trials or research studies. Knowledge of CDISC standards (SDTM, ADaM). Knowledge, Skills, and Abilities
Strong programming and problem-solving skills. Attention to detail and ability to perform rigorous quality checks. Effective communication and collaboration skills to work cross-functionally. Ability to lead projects and provide mentorship.
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