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Director, Clinical Sciences, Oncology

Cambridge, Massachusetts💼 Full-time💰 $183,800–$183,800🗓 2026-06-26 → 2026-07-31

Core

Director-level clinical science leader ensuring data quality and overseeing Phase 1-3 oncology clinical studies to support regulatory submissions and internal governance.

Role type

Senior IC clinical development director (oncology)

Builds

Global clinical trials for oncology therapeutics

Domain

Biotechnology / Oncology / Clinical Development

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

clinical study design, protocol development, data integrity verification, regulatory document authoring, site management, strategic planning, team leadership

Preferred skills

oncology therapeutic knowledge, matrix environment experience, cross-functional collaboration, inspection readiness, investigator engagement

Technologies

clinical protocols, DSUR, INDs, marketing applications, case report forms, data listings, medical coding

Responsibilities

Contribute to regulatory and clinical program strategy and trial design; Author and review clinical study documents in compliance with regulatory standards; Oversee clinical studies and lead data review and analysis; Manage study sites for safety decisions; Participate in start-up and execution of global clinical studies; Develop strategy and messaging for investigator meetings; Train and educate junior clinical science personnel.

Seniority

Director, strategic leadership & hands-on execution

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