Lead Medical Director, Hematology Clinical Development

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

Benefits offered by this job

Relocation support

Discretionary annual bonus

Job summary

Genentech, Inc. in San Francisco, CA seeks a Lead Medical Director to shape the Clinical Development strategy for Phase II–III programs in Oncology & Hematology. You will lead and contribute to CD plans, coordinate with internal and external partners, and support regulatory submissions.

The role is on-site with relocation support. Requirements include 5+ years post-graduate clinical research, 3+ years in late-stage development, and strong clinical monitoring, data interpretation, and scientific

Qualifications

• 5+ years of post-grad clinical/scientific research and/or clinical trial experience.
• 3+ years in biopharmaceutical clinical development with late-stage focus.
• 3+ years of medical monitoring experience in life sciences.
• Strong data analysis, interpretation, and clinical relevance skills.
• Demonstrated scientific writing experience (manuscripts, protocols, regulatory docs).
• Excellent communication for long and short form presentations.

Responsibilities

• Lead the Clinical Development strategy for Phase II–III programs.
• Collaborate with internal/external partners across functions and with regulatory teams.
• Contribute to CDP components (data strategy, publications, KOL development).
• Support regulatory filings and submissions with clinical science input.
• Ensure alignment of CDP with overall CD strategy and annual plans.

Skills

Clinical trial experience

Late-stage development

Medical monitoring

Data analysis

Scientific writing

Cross-functional collaboration

Communication skills

Education

MD/PhD Oncology & Hematology

Job description

Genentech, Inc. in San Francisco, CA seeks a Lead Medical Director to shape the Clinical Development strategy for Phase II–III programs in Oncology & Hematology. You will lead and contribute to CD plans, coordinate with internal and external partners, and support regulatory submissions.

The role is on-site with relocation support. Requirements include 5+ years post-graduate clinical research, 3+ years in late-stage development, and strong clinical monitoring, data interpretation, and scientific