Amgen seeks a Clinical Scientist Director to lead early-phase oncology clinical development, translating scientific strategy into trial execution while ensuring protocol adherence, data integrity, and regulatory compliance across cross-functional teams.
Responsibilities
- Serve as clinical and scientific subject-matter expert for assigned therapeutic area with focus on protocol execution and data integrity
- Conduct medical monitoring activities and assess subject-level clinical data to identify trends, risks, and emerging issues
- Review and analyze clinical trial data for accuracy, completeness, and adherence to protocol and regulatory requirements
- Support cross-functional development of study protocols, concept documents, and clinical strategy implementation
- Oversee collaborators, consultants,



and CROs in completion of key projects and clinical trial delivery

Requirements
- Doctorate degree and 4 years life sciences/healthcare experience, or Master's degree and 7 years, or Bachelor's degree and 9 years
- 5 years pharmaceutical clinical drug development experience
- Early-phase oncology drug development background in industry or academia
- Clinical trial design, monitoring, and implementation expertise with Good Clinical Practice compliance
- Strong written and oral communication skills for scientific concepts and data to leadership
- Experience with clinical data analysis tools and regulatory submission documents

📌 Clinical Scientist Director, Early Development Oncology (España)
🏢 Amgen
📍 España