Overview In this role you drive late-phase oncology development by turning scientific strategy into executable clinical trials. You lead protocol execution, data quality, and cross-functional collaboration to produce decision-ready data that informs regulatory decisions. You will be a scientific expert across the therapeutic area, guiding investigators, CROs, and internal teams while ensuring compliance with ICH-GCP and Amgen standards. This position offers impact at scale, shaping oncology program outcomes and patient care through rigorous data-driven leadership. Compensaciones / Ventajas * Retirement and Savings Plan with company contributions * group medical, dental and vision coverage * life and disability insurance * flexible spending accounts * stock-based long-term incentives * discretionary annual bonus Responsabilidades * Oversee protocol execution and clinical trial integrity across late-phase oncology studies * Lead medical data review and ensure data quality to support decision-ready analyses * Collaborate with cross-functional teams to translate strategy into study concepts and protocols * Provide clinical input on trial design, governance, and regulatory-aligned documentation * Manage relationships with collaborators, consultants, and CROs for key projects * Monitor subject-level data for trends, risks, and issues; manage data monitoring plans * Review and interpret trial results,



ensuring regulatory and protocol adherence * Contribute to data readouts and final reporting, including data cleaning and database lock * Prepare and present information to leadership and external audiences Requisitos principales * Doctorate degree with 4+ years in life sciences/healthcare, OR Master’s with 7+ years, OR Bachelor’s with 9+ years * 5 years of pharmaceutical clinical drug development experience (preferred) * Experience in late-phase oncology drug development * Strong communication and presentation skills for leadership committees (written and oral) * Experience designing, monitoring, and implementing oncology clinical trials, compliant with GCP and regulatory requirements * Experience in clinical data analysis and data readout activities (data cleaning, database lock, data extraction) * Experience drafting high-level regulatory submission documents and clinical responses * Contributing author experience in scientific publications and conference presentations * Experience with data analysis tools (e.g., Spotfire) * strong communication skills * presentation ability * leadership and cross-functional collaboration * Good Clinical Practice (GCP) and regulatory compliance * Clinical trial design and governance * Data monitoring and data quality assessment

📌 Clinical Scientist Director - Late Development Oncology (Barcelona)
🏢 Amgen
📍 Barcelona