Senior Clinical Scientist Director, Early Oncology

Amgen Inc. (IR); España; Híbrido; EUR 131.000 - 177.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Retirement plan

Medical, dental and vision coverage

Stock-based incentives

Flexible work models

Descripción de la vacante

Amgen seeks a Clinical Sciences Director for Early Development in Oncology to translate strategy into execution across trials. You will lead cross‑functional teams, oversee protocol execution, medical data review, and data quality to enable decision‑ready results.

You will contribute to trial design, regulatory interactions, and data interpretation while guiding external collaborators and CROs, with a strong emphasis on data integrity and scientific leadership.

Formación

• Doctorate degree and 4 years of life sciences/healthcare experience
• Master’s degree and 7 years of life sciences/healthcare experience
• Bachelor’s degree and 9 years of life sciences/healthcare experience

Responsabilidades

• Translate scientific and clinical strategy into actionable execution across clinical trials
• Oversee protocol execution, medical data review, and data quality to enable high‑quality, decision‑ready data
• Collaborate within cross‑functional teams to ensure trials meet protocol, regulatory expectations and Amgen standards
• Provide guidance in identifying collaborators, consultants, and CROs for key projects
• Review and analyze clinical trial data to ensure accuracy, completeness and regulatory compliance

Conocimientos

Clinical trial oversight

Data analysis

Regulatory knowledge

Scientific writing

Cross-functional collaboration

Educación

Doctorate degree

Master’s degree

Bachelor’s degree

Herramientas

Spotfire

Descripción del empleo

Amgen seeks a Clinical Sciences Director for Early Development in Oncology to translate strategy into execution across trials. You will lead cross‑functional teams, oversee protocol execution, medical data review, and data quality to enable decision‑ready results.

You will contribute to trial design, regulatory interactions, and data interpretation while guiding external collaborators and CROs, with a strong emphasis on data integrity and scientific leadership.