Overview
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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 / Incentivos
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 xqbhyrx 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 (Granada)
🏢 Amgen
📍 Granada