Senior Statistical Programmer I
Responsibilities
• The Senior Statistical Programmer I will assist the US and/or EU Early Phase Statistical Programming teams by developing SAS programs for analysis datasets.
• They will be responsible for listing and safety summary tables, providing project tracking information to the team, addressing any validation comments, documenting programming activities, acting as a subject matter expert (SME) within the SAS Programming team, and mentor/train other junior team members.
• Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines, and to the highest standard of quality.
• Program analysis datasets, listings, and tables without supervision.
• Serve in a client-facing capacity that demonstrates the ability to anticipate client needs and implement innovative solutions.
• Facilitate flow of information on study budgets and change order management in a timely and efficient manner.
• Liaise effectively with other ICON functions (example: Data Management).
• Set-up and maintain the programming and validation log according to the procedures for Planning, Executing, Tracking, and Documentation of Programming and Validation activities.
Requirements:
• 5+ years of statistical programming experience with working knowledge of data structures (SDTM & ADaM).
• Experience in clinical research (preferably in a CRO setting).
• Experience leading studies while managing timelines, resources, and overall quality in a client-facing capacity.
• Working knowledge of the development and use of standard programs and macros.
• SAS programming skills.
• Bachelor's degree (in a quantitative or scientific discipline).
Responsibilities
• The Senior Statistical Programmer I will assist the US and/or EU Early Phase Statistical Programming teams by developing SAS programs for analysis datasets.
• They will be responsible for listing and safety summary tables, providing project tracking information to the team, addressing any validation comments, documenting programming activities, acting as a subject matter expert (SME) within the SAS Programming team, and mentor/train other junior team members.
• Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines, and to the highest standard of quality.
• Program analysis datasets, listings, and tables without supervision.
• Serve in a client-facing capacity that demonstrates the ability to anticipate client needs and implement innovative solutions.
• Facilitate flow of information on study budgets and change order management in a timely and efficient manner.
• Liaise effectively with other ICON functions (example: Data Management).
• Set-up and maintain the programming and validation log according to the procedures for Planning, Executing, Tracking, and Documentation of Programming and Validation activities.
Requirements:
• 5+ years of statistical programming experience with working knowledge of data structures (SDTM & ADaM).
• Experience in clinical research (preferably in a CRO setting).
• Experience leading studies while managing timelines, resources, and overall quality in a client-facing capacity.
• Working knowledge of the development and use of standard programs and macros.
• SAS programming skills.
• Bachelor's degree (in a quantitative or scientific discipline).
