Senior Clinical Scientist Director, Early Oncology

Amgen

Polska

Hybrid

PLN 523,000 - 708,000

Full time

14 days+

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Benefits offered by this job

Competitive benefits
Career development opportunities

Job summary

Amgen Inc. is seeking a Clinical Sciences Director – Early Development, Oncology to translate scientific strategy into actionable execution across early-phase trials.

You will serve as a key clinical and scientific SME, guiding protocol execution, data review, and quality across cross-functional teams. You will drive medical monitoring, assess subject-level data for trends and risks, and support CROs and collaborators while maintaining governance and regulatory standards.

Qualifications

  • Doctorate degree and 4+ years of life sciences/healthcare experience OR Master’s degree and 7+ years OR Bachelor’s degree and 9+ years.
  • Proven track record in pharmaceutical clinical drug development, especially oncology.
  • Strong communication and presentation skills to leadership committees.

Responsibilities

  • Support early phase clinical development by translating strategy into executable actions across trials.
  • Act as clinical and scientific SME for oncology with emphasis on protocol execution and data integrity.
  • Collaborate with cross-functional teams to ensure trial governance and regulatory compliance; monitor data quality and trends.

Skills

Strategic clinical leadership
Oncology clinical development
Clinical trial design & monitoring
Regulatory knowledge
Data analysis tools (Spotfire)

Education

Doctorate degree in life sciences
Master’s degree in life sciences
Bachelor’s degree in life sciences

Tools

Spotfire
Clinical data analysis tools

Job description

Amgen Inc. is seeking a Clinical Sciences Director – Early Development, Oncology to translate scientific strategy into actionable execution across early-phase trials.

You will serve as a key clinical and scientific SME, guiding protocol execution, data review, and quality across cross-functional teams. You will drive medical monitoring, assess subject-level data for trends and risks, and support CROs and collaborators while maintaining governance and regulatory standards.

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