Sr. Clinical Research Associate, Biospecimen Management

Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology. The company's platform combines advances in visualization of molecular interactions, computational chemistry, and data integration to design orally available small-molecule medicines intended to overcome 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 in February 2023. With offices in California and Shanghai, Structure Therapeutics operates at the center of life sciences innovation in the United States and China.

Structure Therapeutics is seeking a Senior Clinical Research Associate in Biospecimen Management to join our Clinical Operations team. Reporting to the Senior Manager, Biospecimen Management, this role independently manages laboratory and biospecimen operations for assigned clinical studies and may support multiple studies within a program.

The Senior Clinical Research Associate translates sample analysis requirements into executable plans, oversees laboratory vendors, and maintains control of sample flow, reconciliation, analysis status, and storage. This role leads resolution of study-level issues, keeps stakeholders informed of risks and decisions, and mentors less-experienced team members while escalating program-level, contractual, or strategic matters.

• Lead biospecimen and laboratory operations for assigned studies from study start-up through closeout.
• Translate protocols and sample analysis plans into operational timelines, deliverables, and clear vendor requirements in collaboration with Clinical Development and Translational Sciences.
• Lead development and review of laboratory manuals, sample collection guidance, kit specifications, and related operational documents.
• Confirm alignment among protocols, laboratory documents, data requirements, vendor capabilities, and overall study timelines.
• Maintain study-level risk and issue plans, implement mitigations within the role's authority, and elevate material risks with recommended actions.

• Provide day-to-day oversight of central laboratories, specialty laboratories, bioanalytical vendors, biomarker vendors, and short/long term storage partners for assigned studies.
• Lead routine governance meetings and hold vendors accountable for deliverables, quality expectations, timelines, and documented actions.
• Monitor vendor performance indicators and trends; lead investigation, escalation, and resolution of performance issues.
• Review scopes of work, budgets, invoices, change orders, and assumptions for operational accuracy and elevate contractual or budget decisions to the biospecimen lead.
• Contribute subject-matter input to requests for information, requests for proposal, proposal evaluations, and bid-defense meetings.

• Oversee collection, processing, shipment, receipt, tracking, reconciliation, analysis, and storage of samples across assigned studies.
• Establish and maintain study-level sample tracking and reconciliation plans with laboratories, Data Management, and study teams.
• Analyze sample metrics and discrepancy trends, lead root-cause assessment, and drive corrective actions to closure.
• Manage risks related to sample integrity, stability, consent restrictions, chain of custody, and shipment conditions in partnership with relevant functions.
• Ensure biospecimen records, decisions, and vendor deliverables are complete, accurate, and inspection-ready.

• Ensure assigned laboratory and biospecimen activities comply with protocols, ICH Good Clinical Practice, applicable regulatory requirements, and company standard operating procedures.
• Lead preparation of biospecimen documentation for audits and inspections and coordinate timely responses to observations or follow-up requests.
• Contribute to standard operating procedures, templates, metrics, and process improvements for biospecimen management.
• Provide clear study updates and recommendations to Clinical Operations, Clinical Development, Translational…