Biomedical Data Analyst at Cornerstone TTS
Fort Worth, TX
About the Job
CornerStone Technology Talent Services (TTS), in partnership with our client is looking for a Biomedical Data Analyst with database, programming, and data visualization experience (i.e. SAS, R, R-shiny, Tableau, etc), 4 or more years of pharmaceutical/biotech experience in drug development . Preferred Doctoral degree or master’s degree with relevant experience, Minimum Master’s degree and 3 years quantitative science experience.
This role will also have the opportunity for the development of data visualization, statistical / machine learning algorithms, and analytic pipeline / package / applications in R/Shiny. The role may provide opportunities to develop leadership skills in clinical development strategy and to address scientific questions through practical quantitative thinking.
Responsibilities:
• Build a comprehensive understanding of Amgen’s data standards structure across stages of development
• Build a comprehensive understanding of the Metadata Repository (MDR) product and design, and identify areas for improvement and expansion
• Develop integrations with the MDR enabling visualization of the standards, compliance reporting, and metrics
• Use SAS Enterprise Guide to develop and maintain SAS programs to extract Data Element Standards and to create datasets, reports, and workbooks
• Develop and maintain VBA programs to post-process SAS output and automate repetitive document/file processing activities
• Support development of machine learning and other statistical model
Basic Qualifications:
• Master’s degree and 3 years quantitative science experience OR
• Bachelor’s degree and 5 years quantitative science experience OR
• Proficient in SAS programming language
• Good understanding of clinical trials and clinical data
• Proficient in R programming language and Shiny app development
Preferred Qualifications:
• Doctoral degree or master’s degree with relevant experience
• 4 or more years of pharmaceutical/biotech experience in drug development
• Proven project leadership experience
• Experience in designing, analyzing, and reporting clinical trials
• Excellent SAS and/or R computing, modeling, and visualization skills
• Experience working with multiple languages in the Shiny environment (for example. JavaScript, CSS, Python, VBA, etc.)
• Independent and self-motivated
• Strong organizational skills such that facilitate multi-tasking in time-sensitive environments
• Strong communication and collaboration skills
This role will also have the opportunity for the development of data visualization, statistical / machine learning algorithms, and analytic pipeline / package / applications in R/Shiny. The role may provide opportunities to develop leadership skills in clinical development strategy and to address scientific questions through practical quantitative thinking.
Responsibilities:
• Build a comprehensive understanding of Amgen’s data standards structure across stages of development
• Build a comprehensive understanding of the Metadata Repository (MDR) product and design, and identify areas for improvement and expansion
• Develop integrations with the MDR enabling visualization of the standards, compliance reporting, and metrics
• Use SAS Enterprise Guide to develop and maintain SAS programs to extract Data Element Standards and to create datasets, reports, and workbooks
• Develop and maintain VBA programs to post-process SAS output and automate repetitive document/file processing activities
• Support development of machine learning and other statistical model
Basic Qualifications:
• Master’s degree and 3 years quantitative science experience OR
• Bachelor’s degree and 5 years quantitative science experience OR
• Proficient in SAS programming language
• Good understanding of clinical trials and clinical data
• Proficient in R programming language and Shiny app development
Preferred Qualifications:
• Doctoral degree or master’s degree with relevant experience
• 4 or more years of pharmaceutical/biotech experience in drug development
• Proven project leadership experience
• Experience in designing, analyzing, and reporting clinical trials
• Excellent SAS and/or R computing, modeling, and visualization skills
• Experience working with multiple languages in the Shiny environment (for example. JavaScript, CSS, Python, VBA, etc.)
• Independent and self-motivated
• Strong organizational skills such that facilitate multi-tasking in time-sensitive environments
• Strong communication and collaboration skills