Senior Clinical Scientist Director, Late-Stage Oncology

Amgen; Lisboa; Presencial; EUR 120 000 - 160 000; Tempo integral

Resumo da oferta

Amgen is seeking a Clinical Scientist Director for Late Development Oncology Thoracic. The role focuses on translating scientific strategy into actionable execution across late-phase trials, providing hands-on oversight of protocol execution, medical data review, and data quality to enable decision-ready results.

The position requires leadership in cross-functional teams, strong communication skills, and track record in oncology drug development, with say in study concepts, regulatory

Qualificações

• Doctorate, Master’s, or Bachelor’s with life sciences/healthcare experience as required.
• Senior-level qualifications include years of clinical drug development experience.

Responsabilidades

• Serve as clinical and scientific SME for oncology/thoracic area with focus on protocol execution and data integrity.
• Contribute to medical monitoring activities and assess subject-level data for trends and risks.
• Present information to leadership and cross-functional teams, managing issues across functions.
• Guide in identifying collaborators, consultants, and CROs for key projects.
• Translate clinical strategy into study concepts, protocols, and related documents.
• Ensure protocol governance and regulatory alignment throughout development lifecycle.
• Provide clinical input on trials, data review, and interpretation of results.
• Review trial data for accuracy and adherence to protocol and regulatory requirements.
• Conduct data quality assessments within the data monitoring plan to sustain high standards.

Conhecimentos

Leadership

Communication

Presentation skills

Cross-functional collaboration

Clinical data analysis

Formação académica

Doctorate degree

Master's degree

Bachelor's degree

Ferramentas

Spotfire

Descrição da oferta de emprego

Amgen is seeking a Clinical Scientist Director for Late Development Oncology Thoracic. The role focuses on translating scientific strategy into actionable execution across late-phase trials, providing hands-on oversight of protocol execution, medical data review, and data quality to enable decision-ready results.

The position requires leadership in cross-functional teams, strong communication skills, and track record in oncology drug development, with say in study concepts, regulatory