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 (Islas Baleares)
🏢 Amgen
📍 Islas Baleares