Clinical Scientist Director
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Overview
In this role you drive late-phase oncology development by turning scientific strategy into executable clinical trials. You lead protocol execution, data quality, and cross-functional collaboration to produce decision-ready data that informs regulatory decisions. You will be a scientific expert across the therapeutic area, guiding investigators, CROs, and internal teams while ensuring compliance with ICH-GCP and Amgen standards. This position offers impact at scale, shaping oncology program outcomes and patient care through rigorous data-driven leadership.
Compensaciones / Beneficios
- Retirement and Savings Plan with company contributions
- group medical, dental and vision coverage
- life and disability insurance
- flexible spending accounts
- stock-based long-term incentives
- discretionary annual bonus
- Oversee protocol execution and clinical trial integrity across late-phase oncology studies
- Lead medical data review and ensure data quality to support decision-ready analyses
- Collaborate with cross-functional teams to translate strategy into study concepts and protocols
- Provide clinical input on trial design, governance, and regulatory-aligned documentation
- Manage relationships with collaborators, consultants, and CROs for key projects
- Monitor subject-level data for trends, risks, and issues; manage data monitoring plans
- Review and interpret trial results, ensuring regulatory and protocol adherence
- Contribute to data readouts and final reporting, including data cleaning and database lock
- Prepare and present information to leadership and external audiences
- Doctorate degree with 4+ years in life sciences/healthcare, OR Master’s with 7+ years, OR Bachelor’s with 9+ years
- 5 years of pharmaceutical clinical drug development experience (preferred)
- Experience in late-phase oncology drug development
- Strong communication and presentation skills for leadership committees (written and oral)
- Experience designing, monitoring, and implementing oncology clinical trials, compliant with GCP and regulatory requirements
- Experience in clinical data analysis and data readout activities (data cleaning, database lock, data extraction)
- Experience drafting high-level regulatory submission documents and clinical responses
- Contributing author experience in scientific publications and conference presentations
- Experience with data analysis tools (e.g., Spotfire)
- strong communication skills
- presentation ability
- leadership and cross-functional collaboration
- Good Clinical Practice (GCP) and regulatory compliance
- Clinical trial design and governance
- Data monitoring and data quality assessment
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