The Staff Accountant will be responsible for full-cycle general ledger accounting, ERP management, and financial reporting analysis. This role involves ensuring timely compliance with accounting policies, assisting with external audits, and collaborating with various departments to maintain accurate financial data.

The Director of GCP Quality Assurance at Spyre Therapeutics leads Clinical Quality Assurance activities, ensuring compliance with GCP, GLP, and PV regulations. They manage audits, address quality issues, and oversee inspections, while collaborating with clinical development teams to identify compliance risks and improve practices. This role is crucial for maintaining the quality and integrity of clinical studies.

The Director of Biostatistics oversees statistical activities for clinical trials, including trial design, statistical section authoring, and data analysis interpretation. This role involves leadership of a biometrics team, collaboration with cross-functional teams, and regulatory interactions, ensuring high-quality data and timely project deliverables.

The Associate Director, Biologics Stability leads analytical development and quality control for biologic products, managing stability protocols and GMP compliance. Responsibilities include overseeing laboratory operations, driving analytical strategies, ensuring regulatory compliance, and enhancing quality systems. This role demands strong leadership and communication skills, along with a deep understanding of biologics and good manufacturing practices.