Senior Medical Director, Hematology Clinical Development

Genentech, Inc.; San Francisco (CA); On-site; USD 234,000 - 434,000; Full time

Job summary

Genentech, Inc. is seeking a Lead Medical Director to shape Clinical Development Strategy (CDP) for assigned oncology/hematology programs.

You will lead or contribute to Phase II–III planning and ensure alignment with regulatory timelines, science input, and cross-functional teams. You will oversee data analytics, scientific writing, and publication plans, while collaborating with internal and external stakeholders, including CST and regulatory partners, in a fast-paced, on-site SF Bay Area

Qualifications

• 5+ years of post-grad clinical/scientific research and/or clinical trial experience.
• 3+ years of medical monitoring experience in life sciences.
• 2+ years engaging with clinical sites, PIs, and KOLs.
• Experience in late-stage (Phase II–III) drug development.
• Experience contributing to regulatory submissions and scientific documentation.

Responsibilities

• Support the development and implementation of the Clinical Development Plan (CDP) for assigned molecule(s)/indication(s).
• Collaborate with internal/external partners and multidisciplinary teams across functions.
• Participate in meetings to provide clinical input for early development and review Phase I/II protocols.
• Lead or contribute to strategic CD planning and alignment with CD strategy and LCP.
• Contribute to regulatory filings and other regulatory documentation with CST and partners.

Skills

Clinical trial experience

Medical monitoring

KOL engagement

Data analysis

Scientific writing

Education

MD/PhD in Oncology & Hematology

Board Certified/Board Eligible

Job description

Genentech, Inc. is seeking a Lead Medical Director to shape Clinical Development Strategy (CDP) for assigned oncology/hematology programs.

You will lead or contribute to Phase II–III planning and ensure alignment with regulatory timelines, science input, and cross-functional teams. You will oversee data analytics, scientific writing, and publication plans, while collaborating with internal and external stakeholders, including CST and regulatory partners, in a fast-paced, on-site SF Bay Area