Jobs at Structure Therapeutics

The Principal Data Scientist will lead the development of AI-powered data science tools, collaborating with cross-functional teams to enhance clinical research and optimize trials. Responsibilities include designing scalable solutions, ensuring software reliability, and communicating insights effectively.

The Data Scientist will enhance the platforms, develop tools for clinical research, and ensure reliability of analytical solutions using software engineering best practices.

The Sr. Director of Commercial Supply Chain leads supply chain operations, ensuring steady drug supply, demand forecasting, and cross-functional collaboration for clinical and commercial programs.

Lead end-to-end semi-monthly payroll for US employees via ADP TotalSource, coordinate EMEA payroll, process off-cycle and equity taxable events, ensure payroll tax compliance and SOX controls, prepare payroll journal entries and reconciliations, review Ramp expense coding, support month-end close and external audit PBC documentation.

Lead global GLP/GMP Quality Assurance strategy to transition from clinical development to commercial readiness. Build and manage GMP QA and QC Compliance teams, oversee audits/inspections, ensure regulatory compliance (FDA, EMA, ICH, NMPA), manage vendor oversight of CROs/CMOs/CDMOs, drive QMS processes (deviations, CAPA, change control, OOS/OOT), and advise executive leadership on quality risk and inspection readiness.

Lead development and governance of Structures Knowledge System: ontologies, semantic enrichments, data catalog, curated datasets, and digital twins. Build and manage data engineering pipelines for AI, enforce FAIR principles, oversee data stewardship and GxP-compliant governance, enable vendor evaluations, and align data roadmaps with Clinical, CMC, R&D, Commercial, and G&A stakeholders.

Lead complex IT programs in R&D and enterprise functions, managing delivery across software development lifecycles. Ensure alignment between technology and business priorities for effective program execution.

The Legal Operations Manager supports contracting activities and patent administration, manages contract workflows, drafts contracts, and coordinates with legal teams.

Support participant recruitment and retention for clinical trials by designing and executing recruitment/retention plans, collaborating with sites/CROs/vendors, engaging advocacy groups, conducting market research on patient barriers, creating site and participant materials, and analyzing trial metrics to optimize enrollment and retention. Travel to sites and meetings (40-50% US-based).