Clinical Trials Statistical Programmer Role
C
Connect Life Sciences
📍 québec, qc, Canada
Job Description
Join the dynamic field of clinical trials as a Statistical Programmer with in-depth SAS programming skills. Focus on TFL programming and improve data submission strategies using CDISC standards.
This position demands a seasoned programmer with at least six years of involvement in clinical trials. You will prepare clinical data for regulatory submissions, review data outputs, and create programming documentation that adheres to CDISC standards. Training and mentoring responsibilities may also be present, enhancing team function.
Key Responsibilities: • Participate in statistical programming activities for submissions • Develop SAS programs based on CDISC or customer specifications • Review and verify programming outputs for submission • Mentor and share insights with the programming team • Follow SOPs for statistical programming tasks
Requirements: • Over 6 years in statistical programming with clinical focus • Educational background in statistics, computer, o...
This position demands a seasoned programmer with at least six years of involvement in clinical trials. You will prepare clinical data for regulatory submissions, review data outputs, and create programming documentation that adheres to CDISC standards. Training and mentoring responsibilities may also be present, enhancing team function.
Key Responsibilities: • Participate in statistical programming activities for submissions • Develop SAS programs based on CDISC or customer specifications • Review and verify programming outputs for submission • Mentor and share insights with the programming team • Follow SOPs for statistical programming tasks
Requirements: • Over 6 years in statistical programming with clinical focus • Educational background in statistics, computer, o...