Senior Director, Clinical Quality

This role safeguards the scientific and regulatory integrity of Denali's clinical development portfolio by leading enterprise-wide GCP and GCLP quality strategy across all functions engaged in clinical research. It sets the vision and direction for Denali's clinical Quality Management System, drives inspection readiness across the organization, and builds the team and processes needed to scale quality oversight as the clinical portfolio grows. Key Accountabilities / Core Job Responsibilities: • Set enterprise-wide GCP/GCLP compliance strategy and quality vision, translating regulatory and business priorities into a risk-based Quality Management System spanning all clinical functions. • Lead and develop the Clinical Quality organization, managing subordinate managers/directors and providing goal setting, growth planning, and performance feedback for the team. • Own the GCP/GCLP audit program, directing audit strategy across CRO/vendor, laboratory, investigational site, and documentation audits. • Escalate and resolve enterprise-level quality risks, partnering with Regulatory Affairs, Clinical, Clinical Operations, and IT leadership to align quality strategy with program execution. • Drive the GCP/GCLP CAPA and Deviation governance process, ensuring systemic issues are identified and resolved at the functional level. • Direct GCP QA oversight of the eTMF, ensuring inspection-ready documentation practices across the portfolio. • Lead development and enterprise-wide implementation of Quality SOPs. • Provide GCP/GCLP quality metrics and strategic risk assessments to Denali senior management. • Lead organizational preparation for Sponsor and Health Authority inspections, serving as the executive point of contact during inspections. Qualifications/Skills: • Typically requires a Bachelor's degree with 12+ years of relevant GCP/quality experience, including 10+ years of people management experience; advanced degree in a health/science-related discipline preferred. • Expert knowledge of ICH E6(R2) GCP guidelines, FDA Code of Federal Regulations, and other global clinical research regulations, with demonstrated ability to interpret and apply these across functions. • Demonstrated experience building and scaling clinical Quality Management Systems and audit programs in a biotech/pharmaceutical setting. • Proven track record leading regulatory inspections and Health Authority interactions. • Strong leadership, communication, and cross-functional influence skills, with experience managing and developing a team of quality professionals. Salary Range: $245,000.00 to $318,000.00 . Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.