Senior Director, Head of Clinical Program Quality & Excellence (TAU)

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use .  I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the Role As the Senior Director, Head of Clinical Program Quality & Excellence (TAU), you will drive a risk-based quality management approach across the Therapeutic Area Unit, strengthening clinical program performance, regulatory confidence, and inspection readiness. You will provide quality leadership to key governance bodies, identify and mitigate emerging risks, and lead the Clinical Program Quality & Excellence team to embed operational excellence, patient safety, data integrity, and global regulatory compliance across clinical trial delivery. Additionally, you will help advance enterprise quality strategies, influence senior stakeholders, and foster a culture of quality by design, accountability, and continuous improvement. You will report into the Vice President, Head of Clinical, Pharmacovigilance and Medical Quality (CPMQ). How You Will Contribute Drive risk-based quality strategies across assigned clinical programs to ensure compliance, patient safety, and reduced development risk Lead quality risk escalation, governance, and reporting, providing actionable insights to support timely, data-driven decisions Oversee investigations of serious breaches, scientific misconduct, and significant quality events, ensuring effective root cause analysis and sustainable corrective actions Ensure continuous inspection readiness and end-to-end compliance across clinical programs Lead global GCP inspection strategy, including submission-related inspections and regulatory agency interactions as a clinical quality SME Develop and execute risk-based audit strategies to identify, assess, and mitigate quality risks across clinical development programs Lead the Clinical Program Quality & Excellence team, embedding proactive quality oversight, inspection readiness, and cross-functional issue resolution across Study Execution Teams Partner with enterprise quality and continuous improvement teams to drive organizational learning and strengthen clinical trial delivery and pharmacovigilance systems Provide strategic counsel to the Head of CPMQ on complex quality challenges, priorities, initiatives, and resource planning Build, develop, and retain a high-performing team through strong leadership, talent development, succession planning, and a culture of accountability Skills and Qualifications Bachelor’s degree in a scientific, medical, health-related, or equivalent discipline; Master’s or PhD preferred 12+ years of experience in the global pharmaceutical industry, including 5+ years in Quality and/or Compliance supporting clinical development programs Advanced knowledge of clinical research and development across the product lifecycle, including development, commercialization, and lifecycle management Deep expertise in GCP regulations, guidelines, and their practical application Experience in clinical portfolio quality oversight, global quality systems, audit programs, regulatory inspections, and quality risk management Experience leading complex investigations, remediation activities, and corrective and preventive action (CAPA) programs Expertise in developing and implementing risk-based quality management and audit strategies Experience supporting health authority inspections and submission-related regulatory activities Knowledge of clinical trial quality systems, inspection readiness, and compliance oversight frameworks Experience leading enterprise transformation initiatives, including quality system integration, operating model evolution, and outsourcing strategies Experience managing global quality organizations and developing high-performing teams Understanding of Pharmacovigilance, Medical Quality, and Clinical Quality processes and systems Commitment to patient safety, data integrity, scientific rigor, and regulatory compliance Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.   For Location: USA - MA - Cambridge - Kendall Square - 500 U.S. Base Salary Range: $212,000.00 - $333,190.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.  U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.  EEO Statement 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 stat