Lead Medical Director, Product Development, Hematology

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.

Pay / Benefits

• salary range: $213,000 – $396,000 (Boston, MA)
• discretionary annual bonus
• benefits as per company policy
• equal opportunity employer
• relocation not provided

Responsibilities

• 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

Key requirements

• Board Certified/Board Eligible MD (MBBS), or MD(MBBS)/PhD in Oncology & Hematology
• 5+ years post-grad clinical/scientific research and/or clinical trial experience
• 3+ years in biopharmaceutical clinical development, with late-stage experience
• 3+ years medical monitoring experience in life sciences
• 2+ years engaging with clinical sites, PIs, and KOLs
• Solid understanding of Phase II–III drug development and track record of contributing to drug development programs
• Demonstrated ability to foster productive, inclusive team culture in fast-paced settings
• Experience with data analysis, interpretation, and clinical relevance; 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

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