Overview

In this role you drive late-phase oncology development by turning scientific strategy into executable trials. You will act as a clinical and scientific expert, overseeing protocol execution, data quality, and cross-functional collaboration to align with regulatory and Amgen standards. You’ll monitor subject-level data to spot trends and risks, and guide CROs and collaborators to deliver high-quality, decision-ready data. Your work directly supports translating research into impactful cancer therapies, contributing to Amgen’s patient-focused mission.

Compensaciones / Incentivos

- comprehensive health and welfare plans
- Retirement and Savings Plan with company contributions
- stock-based long-term incentives
- bonus program
- flexible spending accounts
- award-winning time-off plans

Responsabilidades

- Provide clinical and scientific oversight for late-phase oncology trials and protocol execution
- Ensure data quality and integrity across the trial lifecycle
- Collaborate with cross-functional teams to translate strategy into study concepts, protocols, and governance
- Monitor subject-level data to identify trends, risks, and issues
- Lead data reviews and interpretation to support regulatory-ready submissions and routine clinical decisions
- Manage external partners (CROs, consultants)



and internal stakeholders to ensure timely delivery of key projects
- Contribute to medical monitoring and overall trial data interpretation for safety and efficacy
- Support study data readouts and completion activities (data cleaning, lock, extraction) and drafting regulatory responses

Requisitos principales

- Doctorate, 4+ years in life sciences/healthcare OR Master’s, 7+ years OR Bachelor’s, 9+ years in life sciences/healthcare
- Experience in pharmaceutical clinical drug development, preferably late-phase oncology
- Strong written and oral communication skills for leadership committees
- Experience designing and monitoring oncology clinical trials compliant with GCP and regulatory requirements
- Experience data readouts, data cleaning, database lock, and data extraction
- Ability to author high-level regulatory submission documents and contribute to scientific publications
- Experience with clinical data analysis tools (e.g., Spotfire)

- strong communication & presentation skills
- problem-solving and proactive issue management
- cross-functional collaboration
- designing and monitoring oncology trials
- data review and interpretation of clinical trial results
- compliance with GCP and regulatory requirements

📌 Clinical scientist director – late development oncology (Bilbao)
🏢 Amgen
📍 Bilbao