Sr. Manager/Assoc. Director, Statistical Programming

Structure Therapeutics • South San Francisco, CA

1d

About The Position

Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical-stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location. POSITION SUMMARY The position supports statistical programming for Phase 3 studies and regulatory submissions, ensuring high-quality, compliant deliverables aligned with CDISC standards and global regulatory requirements (e.g., FDA, EMA). The role maintains oversight of work performed by CROs, including review and verification of outputs to ensure accuracy and compliance; contributes to data review and cleaning; and advances internal programming capabilities through development of macros, processes, and automation to improve efficiency and consistency. Operating with a high degree of independence, they partner cross-functionally to ensure high-quality, timely delivery of statistical programming outputs.

Requirements

• Bachelor’s or master’s degree, in Statistics, Mathematics or other related discipline and at least 7 years Pharmaceutical/Biotech programming experience
• Excellent knowledge of CDISC submission requirements regarding SDTM, ADaM , Define.xml, Reviewers Guide and Validation Rules
• Demonstrated experience authoring and reviewing SDRG, ADRG, and dataset specifications (SDTM/ ADaM )
• Ability to develop macros, utilities, and automation to improve programming efficiency
• Expert level SAS programming and management background along with Solid knowledge and experience of SAS Programming language including SAS Base, SAS/Macros, SAS/Graph and SAS/Stat
• Experience overseeing CRO programming activities, including review and verification of deliverables
• Strong interpersonal communication skills to collaborate with colleagues, stakeholders, and vendors effectively and clearly in small biotech setting

Nice To Haves

• Ability to work in a fast-paced, cross-functional environment

Responsibilities

• Provides statistical programming support to Structure’s expanding portfolios
• Support and perform statistical programming for Phase 3 clinical studies and regulatory submissions
• Author and review SDRG, ADRG, and dataset specifications (SDTM and ADaM ) to ensure compliance, traceability, and submission readiness
• Develop, validate , and maintain CDISC-compliant datasets (SDTM and ADaM ) and analysis outputs (TFLs) using SAS (and/or R)
• Ensure timely delivery of high-quality, compliant deliverables aligned with CDISC standards and global regulatory requirements (e.g., FDA, EMA)
• Maintain oversight of work performed by CROs, including review and verification of outputs to ensure accuracy, quality, and compliance
• Perform hands-on programming for complex analyses, ad hoc requests, and critical deliverables as needed
• Review study documents, including protocol, CRFs, SAP, DTS, and TFL shells
• Contribute to data review and cleaning activities to support data integrity and analysis readiness
• Collaborate cross-functionally with Biostatistics, Data Management, Clinical Development, and Regulatory teams
• Develop and implement programming standards, macros, and automation to improve efficiency, consistency, and scalability
• Review datasets, TFLs, and define.xml to ensure quality and adherence to standards and specifications
• Support regulatory submissions, including preparation, validation, and response to health authority queries
• Identify and drive process improvements and best practices in statistical programming
• Operate with a high degree of independence to manage priorities and ensure timely , high-quality deliverables
• Perform other duties and responsibilities as assigned

Benefits

• medical
• dental
• vision insurance
• 401k match
• unlimited PTO
• paid holidays including winter shutdown

What This Job Offers

• Job Type: Full-time
• Career Level: Senior