Experteer Overview
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In this role you will lead medical input across hemato-oncology clinical programs, ensuring scientific rigor and patient safety. You will collaborate with cross-functional teams to design, implement, and monitor AstraZeneca-sponsored studies from early through late phases. You will contribute to regulatory submissions and governance processes, and serve as Medical Monitor for trials. You will drive safety oversight and medical strategy, shaping programs that align with the company’s mission to deliver life-changing medicines.
Compensaciones / Incentivos
• Lead design and implementation of clinical hemato-oncology projects within CPT/CST
• Provide clinical input to trial design, execution, data review and interpretation
• Ensure safety monitoring and ethical/regulatory compliance across studies
• Collaborate with external investigators, KEEs, sites and internal stakeholders to reflect clinical practice and regulatory requirements
• Support regulatory submissions (INDs/BLAs,



safety reports) and EC/IRB interactions
• Develop clinical development plans integrating pre-clinical and early findings
• Present protocols and plans at governance meetings and obtain approvals
• Lead or contribute to cross-asset and cross-indication working groups
• Manage day-to-day operations of assigned drug development projects in hemato-oncology
• Serve as Medical Monitor for Phase I–III studies and influence study governance
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Responsabilidades
• MD or international equivalent
• Minimum 2 years of relevant experience
• Medical hematology-oncology clinical training
• Board Certification preferred
• Experience with design/conduct of oncology/malignant hematology studies in academia, pharma or CRO
• Knowledge of GCP and regulatory frameworks
• Understanding of clinical trials methodology
• Strong communication and presentation skills for leadership forums
Requisitos principales
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📌 Global Development Medical Director, Hematology Oncology (Barcelona)
🏢 AstraZeneca
📍 Barcelona