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The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in the Late-Stage Oncology portfolio. This role involves partnering with clinical colleagues, leading data review strategies, and contributing to regulatory submissions.

The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in support of the development strategy for programs within the Late-Stage Oncology portfolio. Responsibilities include being a clinical development expert, partnering with colleagues for trial implementation, scientific oversight, data analysis, safety profile monitoring, and compliance with regulations and SOPs. Requires a science degree and 7+ years of clinical research experience in industry/CRO, with a focus on phase 3/pivotal space in Oncology.

The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in support of the development strategy for programs within the Late-Stage Oncology portfolio. This role involves managerial responsibilities, protocol authoring, data review, safety analysis, and regulatory document preparation.

The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in the Late-Stage Oncology portfolio. The role involves managing direct reports and contingent workers, collaborating with cross-functional teams, and ensuring compliance with regulations.

The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in support of the development strategy for programs within the Late-Stage Oncology portfolio. This role involves authoring protocols, overseeing data collection and review, analyzing the safety profile of drugs, and ensuring compliance with regulations and standards.

The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in support of the development strategy for programs within the Late-Stage Oncology portfolio. This role involves managing direct reports, partnering with clinical and medical colleagues, and ensuring compliance with regulations and guidelines.

The Late-Stage Clinical Scientist (non-MD, Director) is responsible for scientific oversight, data integrity, and quality of clinical trials in support of the development strategy for programs within the Late-Stage Oncology portfolio. Responsibilities include clinical development expertise, collaboration with cross-functional teams, authoring clinical documents, data review, safety analysis, and compliance with regulations.