Experteer 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
• 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

Responsabilidades
• 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)

Requisitos principales
• 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

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