Principal Statistical Programmer

Tasks

• Design data structure and specifications for deliverables
• Develop and validate SAS programs for clinical trial data
• Develop global tools to improve programming efficiency
• Ensure data quality and accuracy for submissions
• Generate integrated summaries of safety and efficacy
• Lead pooled and exploratory analyses programming
• Plan and report clinical trial exploratory analyses
• Review datasets for submission readiness
• Specify and deliver ISS and ISE datasets
• Support publications and presentations
• Support regulatory agency responses

Perks/Benefits

• Career development
• Flexible working
• Mentorship
• Remote work

Skills/Tech-stack

ADaM | CDASH | CDISC | Clinical data | Clinical data standards | Clinical trials | Data Quality | Data Standards | Define.xml | Exploratory analysis | Pooled Analysis | R | SAS | SAS Macros | SDTM