Jobs at Structure Therapeutics

The intern will assist with event planning, administrative tasks, and lab operations support, requiring strong organizational and communication skills.

The Site Engagement Lead will manage participant recruitment and retention strategies for clinical trials, collaborate with teams, and improve engagement through educational resources and relationships.

The Director of Analytical Development leads analytical activities for late-stage drug development, ensuring compliance with regulatory standards and overseeing method development and qualification. Responsibilities include authoring submissions for regulatory filings and managing cross-functional teams and external partnerships in drug development.

The Legal Summer Intern will assist the Legal and Compliance department in creating compliance training materials and conducting legal research while gaining exposure to in-house legal processes.

Lead in vivo pharmacology studies, troubleshoot experimental challenges, ensure data integrity, and mentor junior scientists while supporting drug discovery projects.

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.

This role involves providing strategic QA oversight of drug substance manufacturing, ensuring GMP compliance, and aligning quality strategies across teams. Responsibilities include document review, deviation management, and vendor interactions.

Join a team focusing on membrane protein expression and purification to support drug discovery. Responsibilities include construct design, GPCR purification for cryo-EM, and data analysis.

Lead CADD/SBDD strategy for discovery programs, translate structural insights into testable design hypotheses, apply CADD methods (docking, MD, FEP+), partner with structural biology, medicinal chemistry, DMPK and platform teams, and mentor scientists to accelerate S-DMTA cycles.

The Director of Research Data Management will define and implement data management strategies, establish data standards, and lead data integration efforts that support drug discovery processes, partnering with various scientific teams.

The Senior Patent Agent will oversee the intellectual property portfolio, draft new applications, guide IP strategies, and support patent prosecution efforts.

The Associate Scientist/Scientist in DMPK will develop bioanalytical methods and analyze samples for small molecule projects, collaborating with cross-functional teams.

The Supply Chain Manager ensures timely supply and procurement of raw materials and drug substances, optimizing operations while meeting compliance and quality standards.

The role focuses on computational chemistry, employing molecular dynamics and cheminformatics for small-molecule drug discovery and optimization. Collaborates with multidisciplinary teams to influence therapeutic design.

The Principal Scientist to Associate Director will oversee analytical development for small molecules, manage CROs and CDMOs, ensure regulatory compliance, and develop strategies for analytical methods and documentation.

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 role involves leading statistical programming for clinical studies, ensuring compliance with CDISC standards, collaborating across teams, and enhancing programming efficiency through automation.

The Associate Director/Director of Biostatistics provides statistical support for clinical drug trials, oversees CRO activities, and ensures regulatory compliance for data submissions.