.Global Clinical Operations Program Director - Haematology Location: Barcelona, Spain (On-site). 3 days working from the office and 2 days working from home. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. Do you have expertise in and a passion for global Clinical Program Management? Would you like to apply your expertise to impact the development of an exciting oncology portfolio in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you! Join a dedicated Oncology team in Haematology that's growing fast and building a strong track record of success. We have multiple indications and many high-quality molecules at all stages of development. What you'll do The Global Clinical Operations Program Director (GPD) is a core global role within the Haematology R&D Clinical Operations function. The span of responsibilities is broad and may support one or several products depending on scope and complexity. The products supported can be in any phase (Early and Late), of development or on the market. On behalf of the Senior Global Clinical Operations Program Director (Sr GPD), the GPD provides strategic operational leadership and oversight of a suite of global clinical studies within a program covering all clinical operations deliverables to scope, quality, budget, time, resource and risk, ensuring new innovative design and delivery models are used appropriately. The GPD may provide project leadership for cross-functional clinical submission teams in support of regulatory marketing applications and post-registration product maintenance deliverables. Additionally, the GPD may lead or contribute to improvement and change projects within clinical operations and/or other business areas, as well as potential line management of clinical operations personnel. Essential for the role Bachelor of Science/Master of Science degree in related discipline, or equivalent work experience. Advanced degree is preferred e.G. PhD, MD, PharmD Experience from within the pharmaceutical industry or similar large multinational Clinical Research organizations. Experience in Oncology Phase 1 dose escalation and/or registrational Phase 3 trials as a global study leader or Oncology Program Manager Proven experience in clinical development/drug development process in various phases of development and therapy areas. Proven knowledge of project management tools and processes Proven ability to learn by working in multiple phases, TAs, and/or different development situations