Associate Director / Sr. Manager, Statistical Programming

Associate Director / Sr. Manager, Statistical Programming

Direct Hire Full-Time Role

Pay Rate: $80 - $90 per hour

Location: Redwood City, CA - Hybrid Role

Job Summary:

The Associate Director/Sr. The Manager of Statistical Programming will have primary responsibility for the planning, execution, and completion of all statistical programming activities.

Duties and Responsibilities:

• Lead and manage statistical programming activities for clinical studies, ensure statistical programming deliverables are delivered within timelines and with high quality and cross-study consistencies.
• Collaborate with Biostatisticians in the creation, implementation, and maintenance of programming for each study, accounting for timelines, resources, and quality deliverables; ensure programming has been carried out per industry and internal standard practice.
• Collaborate with Data Management to implement the CDISC standard at the CRF and database build-up stage; review annotated case report forms.
• Provide technical leadership and guidance to the programming team and vendors around project conventions, standards, best practices, and specifications.
• Provide support in the production/validation of SDTM, ADaM, summary tables, and figures.
• Manage oversight of contractors and CROs.
• Manage statistical programming support of potential FDA/EMEA regulatory submissions, following CDISC standards.
• Contributes to the departmental process.

Requirements and Qualifications:

• A minimum of 6+ years of experience in statistical programming and analysis of clinical trial data with demonstrated increasing responsibility.
• Experience programming for and contributing to an NDA or BLA submission preferred.
• Experience working with CROs.
• Master's degree or above in statistics, data science/analytics, computer science, or other relevant scientific field.

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