Genentech

Overview In this role you will shape and lead the Clinical Development Plan for assigned oncology programs, guiding late-stage strategy and global execution. You will collaborate with cross-functional teams and external partners to align scientific and regulatory goals, driving label-enabling outcomes. You’ll provide clinical input for Phase I–III studies and regulatory submissions, while building data, publications, and KOL strategies. This is a high-impact, fast-paced role at Roche with a focus on meaningful patient outcomes.

Leistungen / Benefits salary range: $213,000 – $396,000 (Boston, MA) discretionary annual bonus benefits as per company policy equal opportunity employer relocation not provided Verantwortungsbereiche Lead or substantially contribute to the Clinical Development strategy and plan (CDP) for assigned molecule(s)/indication(s) Support development and implementation of the CDP, including data analytics and governance components Collaborate with internal and external partners across functions (BD, research, commercial, legal, etc.) Provide clinical science input for early development and Phase I–II protocol reviews Contribute to regulatory filings and regulatory documentation with clinical input Ensure strategic and operational alignment of the CDP with CD strategy and LCP Develop CDP components (analytics/data strategy, KOL development, publications strategy) with CST and sub-teams Zentrale

Anforderungen Board Certified/Board Eligible MD (MBBS), or MD(MBBS)/PhD in Oncology strong scientific writing skills Outstanding interpersonal, verbal, and written communication Influencing and relationship-building across internal and external stakeholders Cross-functional collaboration and proactive issue resolution Data analysis and interpretation Scientific writing (manuscripts, protocols, health authority documents) Regulatory submissions and documentation