Clinical Scientist Director - Late Development Oncology

What You Will Do

• Support late‑phase clinical development by translating scientific and clinical strategy into actionable execution across clinical trials.
• Provide hands‑on oversight of protocol execution, medical data review, and clinical data quality to enable high‑quality, decision‑ready data.
• Work collaboratively within cross‑functional teams to ensure clinical trials are executed in alignment with protocol intent, regulatory expectations, and Amgen quality standards.
• Serve as a clinical and scientific subject‑matter expert for the assigned therapeutic area and disease indication, focusing on protocol execution and data integrity.
• Contribute to medical monitoring activities and support ongoing assessment of subject‑level clinical data to identify trends, risks, and emerging issues.
• Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross‑functional teams.
• Provide guidance and assistance in the identification and management of collaborators, consultants, and/or CROs in completing key projects.
• Translate clinical strategy into the development of study concept documents, study protocols, and related documents.
• Ensure integrity of protocols and related components of clinical plans for delivery of final protocol and its governance approval.
• Provide clinical input into implementation of clinical trials, delivery, clinical data review, and interpretation of results.
• Review and analyze clinical trial data to ensure accuracy, completeness, and adherence to protocol and regulatory requirements.
• Conduct thorough data quality assessments within a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle.

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

• 5 years of pharmaceutical clinical drug development experience.
• Proven track record of clinical trial process improvement.
• Industry or academic experience in late‑phase drug development for Oncology.
• Strong communication and presentation skills to clearly communicate scientific concepts/data to leadership committees both internally and externally, in written and oral formats.
• Experience designing, monitoring, and implementing clinical trials for Oncology and interpreting test results in compliance with Good Clinical Practice standards and regulatory requirements.
• Understanding of conducting study data readout activities, including data cleaning, database lock, data extract, and producing outputs of data.
• Experience drafting high‑level submission documents for regulatory submissions, including authoring clinical regulatory responses for health regulatory interactions.
• Serving as a contributing author to scientific publications and data presentations at scientific conferences.
• Experience in clinical data analysis such as Spotfire or other data analysis tools.

• Competitive benefits and a collaborative culture supporting your professional and personal growth.
• Annual salary range based on qualifications and experience.
• Comprehensive Total Rewards Plan, including health and welfare plans for staff and eligible dependents.
• Retirement and Savings Plan with generous company contributions.
• Group medical, dental, and vision coverage.
• Life and disability insurance.
• Flexible spending accounts.
• Discretionary annual bonus program and long‑term incentive stock‑based awards.
• Flexible work models, including remote and hybrid arrangements where possible.

523139,30

PLN – 707776,70

PLN

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

Please contact us to request accommodation.