Overview

In this role you will guide late-phase oncology development, translating scientific strategy into executable clinical programs. You’ll serve as a clinical and scientific expert, overseeing protocol execution, data quality, and cross-functional collaboration to deliver decision-ready results. You will influence study concepts, protocols, and data interpretation while ensuring regulatory alignment and Amgen standards. This is a chance to shape late-stage oncology programs and directly impact patient outcomes through disciplined trial execution.

Compensaciones / Beneficios

- Retirement and Savings Plan with company contributions
- Group medical, dental, and vision coverage
- Life and disability insurance
- Versátil spending accounts
- Discretionary annual bonus program
- Stock-based long-term incentives

Responsabilidades

- Provide hands-on oversight of protocol execution and clinical data review
- Collaborate across cross-functional teams to align trials with protocol intent and regulatory expectations
- Serve as SME for the therapeutic area with emphasis on data integrity and trial governance
- Identify trends, risks, and issues from subject-level data and support medical monitoring activities
- Guide budget, CROs, and collaborators in key projects and study delivery
- Translate clinical strategy into study concept documents,



protocols, and related governance documents
- Ensure protocol integrity and execution of clinical plans, including governance approvals
- Contribute to data interpretation, results reporting, and regulatory-style submissions

Requisitos principales

- Doctorate with 4+ years life sciences/healthcare experience OR Master with 7+ years OR Bachelor with 9+ years
- Experience in pharmaceutical clinical drug development, preferably late-phase Oncology
- Strong communication and presentation skills to leadership and external audiences
- Experience designing, monitoring, and implementing oncology trials per GCP and regulatory requirements
- Experience in data readouts, data cleaning, database lock, and data extraction for regulatory outputs
- Experience drafting high-level regulatory submission documents and responses
- Experience as contributing author for publications and conference presentations
- Experience with clinical data analysis tools (e.g., Spotfire)

- Strong communication and presentation skills
- Cross-functional collaboration
- Problem solving and risk management
- Clinical trial design and monitoring
- Data quality assessment and data integrity
- Regulatory compliance (GCP, regulatory submissions)

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