Seattle Genetics is seeking a Sr. level SAS programmer to oversee statistical programming activities for multiple Phase I-III clinical studies. The primary focus is to ensure that product and study level deliverables are completed on time, of high quality, and in accordance with company, industry, and regulatory requirements. The secondary focus is to manage salaried and contract programmers.

Functional Role:
The position reports to the Head of Clinical Programming and will function as a Manager, Study Lead Programmer, and Support Programmer.

Responsibilities:
• Accuracy, completeness, quality, and timely delivery of clinical programming deliverables at the product and study level.
• Ensuring programming is conducted according to departmental and industry standards.
• Managing salaried and contract programmers efficiently across studies.
• Contributing to the development of departmental utilities, processes, and procedures.

Activities:
• Manage other salaried and contract programmers of varying levels to provide oversight, guidance, mentoring, feedback, and performance reviews.
• Attend cross-functional clinical study team meetings and lead study programming meetings.
• Interpret study documentation and industry guidance to produce programming requirements and specifications.
• Provide SAS programming support for a variety of activities including but not limited to creating outputs for: integrated analyses, clinical study reports, safety monitoring, manuscripts, conferences, ad hoc analyses, and exploratory analyses.
• Review and provide feedback on deliverables from other clinical groups including: statistical analysis plans; table, listing, and figure shells; data management plans; data transfer plans; electronic data entry screens; and case report forms.
• Set up and maintain programming infrastructure at the product and study level.
• Assist with the development, maintenance, and presentation of standard macros, utilities, processes, procedures, guidelines, and training materials to support a variety of activities in the Clinical Programming group.