Senior Director and Head of Clinical Program Quality

Clinical Programs Quality Leadership

Leads the global Clinical Programs Quality organization, establishing strategic leadership and oversight of Takeda's clinical development programs and ensuring risk-based quality interventions and audits are performed for timely mitigations. Provide quality oversight of R&D's strategic suppliers and service providers, ensuring outsourced activities are carried out with high quality and compliance. Promotes inspection readiness for clinical trials and strategic supplier activities, ensuring preparations, management of and response to clinical pre-approval inspections are resourced, prioritized, and expeditiously reported. Serves as a senior strategic Quality Partner to relevant R&D stakeholders and strategic suppliers. Reports to the Head of CPMQ and is a key member of the CPMQ Leadership Team, contributing to the design, implementation and advancement of the CPMQ strategy, model and operations.

Develop, implement, and refine a proactive quality oversight model for Takeda's clinical development programs and strategic suppliers, ensuring compliance with Takeda standards and applicable regulatory requirements. Leads the Clinical Programs Quality function in the development, implementation and refinement of a proactive quality oversight model for Takeda's clinical development programs across the TAUs and Business Units, ensuring compliance with Takeda standards and applicable regulatory requirements. Ensures a robust and risk-based audit strategy and framework for the clinical development programs including program- or study-level audits and investigator site audits, is developed and implemented in a timely manner, communicating any critical compliance risks to Management, and ensuring that corrective and preventive actions are implemented. Actively participates in Takeda R&D's clinical trial delivery oversight and operating model improvements and enhancements, championing clear accountabilities, continual improvement and mitigations for past risks. Ensures the identification, investigation and timely mitigation of quality issues and risks at the development programs and studies. Escalates these issues to senior management. Establish effective mechanisms to monitor compliance, issue, and risk management of development programs and strategic suppliers, ensuring timely mitigations. Analyzes information gathered in the oversight of the development programs to inform R&D Quality and other stakeholders of any actionable insights and to promote a state of compliance. Ensures knowledge management and lessons learned are shared and applied across development programs. Supports R&D to be inspection ready with a culture of sustainable compliance. Represents Takeda as a clinical quality subject matter expert during health authority inspections of the sponsor. Provides strategic direction to assure that responses are timely and appropriate to maintain Takeda's good standing with regulatory agencies. Ensure that all clinical inspection commitments are fulfilled on time. Serve as a strategic thought partner to the Head of CPMQ with regard to complex problems affecting development activities, with an eye to current and future initiatives, strategies, and budgets. Ensures any quality or compliance risks and opportunities are communicated to the GPTs and relevant sub-teams, so that the teams are well-informed to make decisions on quality and compliance priorities. Contributes to the Clinical & Safety Quality Council. Lead and participate in governance / quality councils relevant to clinical and supplier activities, contributing to continual improvements and successes. Establishes Quality Agreements with strategic suppliers and and governance meetings e.g., Quality Management Working Group, etc. Ensures robust talent development and succession planning measures are in place to promote organizational growth / elevate capabilities.

Scientific or allied health / medical degree (BSc). Masters / PhD preferred. Minimum of 12 years of increasing responsibility and relevant experience in the global pharmaceutical industry, preferably with at least 5 years of Quality / Compliance experience. Advanced knowledge of clinical research (GCP), pharmacovigilance (GVP) and medical throughout R&D and commercialization, and relevant regulations. Preferably with experience in strategic roles involving quality systems and clinical portfolio oversight, large-scale audit programs, regulatory inspection management, investigation and remediation activities on a global level and successful management of business transformation / change management initiatives e.g., quality system integration, outsourcing strategy, etc. Fluency in written and spoken English, additional language skills a plus.

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.