Experteer Overview
Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.
In this high-impact role, you will lead medical development activities for hematology/oncology programs, guiding clinical strategy from early to late-stage development. You will work cross-functionally with CPT, GST, and external experts to ensure scientifically rigorous programs and timely regulatory submissions. You will monitor safety as Medical Monitor and mentor junior staff, shaping the medical content of protocols and regulatory documents. This is an opportunity to influence pipeline decisions and deliver transformative cancer therapies.
Compensaciones / Ventajas
• Provide scientific input into trial design and execution for hematology/oncology programs
• Lead or participate in Clinical Product Team and Clinical Sub-Team activities
• Ensure safety monitoring and high ethical standards in line with GCP and regulatory requirements
• Develop and defend clinical development plans and governance for compounds/programs
• Mentor less experienced team members and potentially manage physicians or scientists
• Collaborate with global medical affairs, marketing,



and cross-functional teams to integrate clinical input into protocols
• Prepare regulatory documents (Dossiers, BLAs, INDs) and responses to regulatory questions
• Oversee the development and delivery of clinical study reports and regulatory submissions
• Contribute to due diligence for in-licensing and cross-asset program initiatives
• Present protocols and development plans at governance forums
• Support escalation of opportunities and ESRs as needed
• Contribute to quality improvements in clinical programs and processes
• Serve as Medical Monitor and medical expert for Phase I–III studies
• Lead training for investigators xqbhyrx and monitors
Responsabilidades
• MD or international equivalent
• Medical hematology-oncology clinical training
• Minimum 4 years of relevant experience
• Board Certification preferred
• Significant clinical research experience in oncology/malignant hematology
• Detailed knowledge of GCP and regulatory guidelines
• Understanding of regulatory approval processes and pharmaceutical Ru0026D operations
• Ability to lead complex plans and collaborate across functions
• Strong communication and presentation skills
Requisitos principales
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📌 Global Development Senior Medical Director, Hematology Oncology (Barcelona)
🏢 AstraZeneca
📍 Barcelona