Senior Director, Regional Site Management and Monitoring

Senior Director, Regional Site Management and Monitoring (SMM) Cell Therapy We are currently seeking a Senior Director, Regional Site Management and Monitoring (SMM), Cell Therapy, to be responsible for delivering the Cell Therapy clinical interventional studies in Australia. About AstraZeneca AstraZeneca is committed to bold innovation, collaboration, and putting patients at the heart of every decision. Through our newly established Cell Therapy team in Australia, we’re redefining how advanced therapies reach those who need them most. What You'll Do In this pivotal leadership position, you will head up our dedicated Cell Therapy group for Australia—shaping team culture, driving engagement and developing a high‑performing, patient‑focused team. Working cross‑functionally across key therapy areas, operations, medical affairs, technology and AI, you’ll build strong partnerships that enable seamless delivery of Cell Therapy studies and ultimately, better patient outcomes. You’ll oversee end‑to‑end study execution across the region, ensuring resources, timelines, quality standards and budgets are consistently met. As a trusted partner to local study managers, you’ll guide feasibility assessments, forecast timelines and recruitment needs, strengthen site readiness and maintain the highest levels of compliance. You will champion process improvement, support digital innovation, and ensure studies remain “inspection‑ready” at all times. A critical part of your role will be developing and coaching your team, modelling AstraZeneca’s values and embedding a culture of excellence, collaboration and innovation. You’ll also cultivate strong relationships with CROs, vendors and global partners to ensure fast, high‑quality delivery of complex Cell Therapy trials. What You Will Bring You have a strong foundation in life sciences and extensive experience in clinical or development operations—ideally 7+ years leading teams within highly regulated, fast‑moving environments. You are an inclusive, empowering leader who knows how to grow capability, guide through change and inspire high performance. With deep operational and technical experience, you’re confident navigating complex study delivery challenges and making sound decisions that keep patients at the centre. You excel at building trusted partnerships, influencing stakeholders and communicating clearly across all levels of the organisation. Naturally organised and analytical, you bring strong project and resource management capabilities, financial acumen and a sharp eye for detail—balanced with the ability to prioritise and delegate effectively. You’re comfortable with digital tools, communicate fluently in English, and have the flexibility to travel within the region. Success in this role is supported by strong knowledge of clinical study processes, GMP/ICH/GCP guidelines, monitoring, data management and drug‑handling procedures. Experience working with CAR‑T or Cell Therapy trials is highly desirable, as is familiarity with global and local regulatory requirements. You’re someone who looks for smarter, more efficient ways to deliver clinical trials—improving quality, reducing timelines and optimising budget without compromising standards. You thrive in cross‑functional, cross‑cultural environments and work confidently with remote teams. With strong integrity, sound judgement and the ability to navigate challenging situations, you operate to the highest global standards and bring a steady, solution‑focused mindset. Why AstraZeneca At AstraZeneca we’re dedicated to being a Great Place to Work, where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society, in an inclusive culture that champions diversity and collaboration and is always committed to lifelong learning, growth and development. EEO Statement AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible. We welcome and consider applications from all qualified candidates, regardless of their characteristics, and comply with all applicable laws and regulations on non‑discrimination in employment. We recognise that any recruitment process may present challenges; if there is anything we can do to make our recruitment process more accessible for you, please let us know via this Form. Date Posted: 24‑Nov‑2025 | Closing Date: 18‑Dec‑2025 Visit our website: #J-18808-Ljbffr