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 / Beneficios Retirement and Savings Plan with company contributions group medical, dental and vision coverage life and disability insurance adaptable 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 (Valencia)
🏢 Amgen
📍 Valencia