Associate Director, Statistical Programming- Job ID: 1150 at Ascendis Pharma | Torre
Associate Director, Statistical Programming- Job ID: 1150
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Ascendis Pharma

Associate Director, Statistical Programming- Job ID: 1150

Ascendis Pharma
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Full-time
Compensation
USD180k - 210k/year
location_on
Hybrid (Palo Alto, CA)
Posted about 3 years ago

Responsibilities

Ascendis Pharma is a fast-growing, dynamic biopharmaceutical company with Headquarters in Denmark that offers you room to grow and the freedom to take responsibility and make a difference for patients every day. Ascendis Pharma is looking for an Associate Director, Statistical Programming to lead and support statistical programming activities for drug development. The role involves managing internal and external resources, providing programming support to statisticians, and ensuring compliance with CDISC standards. The position requires a comprehensive knowledge of SAS, project and resource management, regulatory filing experience, and a broad understanding of the pharmaceutical drug development process. The Associate Director will also provide statistical programming expertise on process improvement initiatives and manage projects with partner and functional service providers. The position is based in Palo Alto, CA and may be remote. The salary range is estimated to be $180,000 - $210,000 per year. Responsibilities: - Manage internal and external resources to lead or support assigned project statistical programming activities - Provide programming support to statisticians in production of summary tables, data listings, and graphs required for clinical trials - Develop SAS code and table templates for preparing, processing, and analyzing clinical data - Interact with project teams, statisticians, and data management personnel to establish project timelines and perform statistical analyses - Manage assigned project programming activities to ensure timely delivery of tables and data listings - Provide guidance and QC/QA standards to ensure quality of deliverables - Represent the Statistical Programming team as study lead, focusing on data integrity, collaboration, and on-time deliverables - Manage and provide oversight of Statistical Programming FTEs, contractors, and CROs - Process clinical data required for statistical analysis - Provide support in production of summary tables, data listings, and graphs required for trial report and clinical development, and CDISC datasets for regulatory submission
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