Experteer Overview
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In this role, you will contribute to and lead scientific input across early and/or late-phase AstraZeneca-sponsored programs within hematology, collaborating with cross-functional teams to translate clinical strategy into study design and execution. You will drive data interpretation, regulatory submissions, and global registration activities while upholding GCP and high ethical standards. The position offers exposure to immunotherapy and cell therapy programs and opportunities to influence cross-asset development efforts. You will work in a matrix environment to deliver impactful medicines for patients with hematological cancers.
Compensaciones / Incentivos
• Translate clinical strategy into study concepts, protocols, and related documents within CPT
• Provide clinical/scientific input for trial design and execution, including immunotherapy and cell therapy studies
• Build internal and external relationships with clinical teams, regulators, and external service providers
• Ensure scientific accuracy of protocols and components of clinical plans, and governance-approved final protocols




• Lead development of protocols and clinical study reports to meet GCP, ICH, and AstraZeneca standards
• Manage cross-functional projects to advance drugs through all development phases, acting as a technical expert
• Review medical and trial data to draw conclusions with Medical Director
• Support regulatory submissions and clinical components of regulatory documents
• Participate in ESR reviews and manage site communications for ICF changes and EC/IRB questions
• Contribute to investigator training and on-site supervision activities xqbhyrx
Responsabilidades
• BS with strong experience in drug development, preferably hematology/haematology
• Minimum of 5 years relevant industry or academic experience in drug development
• Experience in malignant haematology clinical trials preferred
• Technical knowledge to interact confidently with internal and external partners
• Foundational knowledge of FDA/major regulatory environments and GCP requirements
• Understanding of medical monitoring, regulatory approvals, and Ru0026D operations
Requisitos principales
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📌 Global Development Director Scientist (Barcelona)
🏢 AstraZeneca
📍 Barcelona