Lead Medical Director, Hematology Clinical Development

LumiraDx Limited; Boston (MA); On-site; USD 213,000 - 396,000; Full time

Job summary

Genentech is seeking a Lead Medical Director for on-site roles in Boston, MA, responsible for shaping the Clinical Development Plan (CDP) for assigned molecules and ensuring alignment with overall strategy. You will collaborate with cross-functional teams, provide clinical input for early development and Phase II/III protocols, and contribute to regulatory submissions.

The role requires MD/PhD with oncology/hematology focus, 5+ years of clinical/research experience, and 3+ years in late-stage

Qualifications

• Board Certified/Board Eligible MD/PhD in Oncology & Hematology.
• 5+ years post-grad clinical/scientific research and/or clinical trial experience; 3+ years in biopharmaceutical clinical development (late stage).
• 3+ years of medical monitoring experience in life sciences.
• 2+ years engaging with clinical sites, PIs, KOLs, etc.
• Solid understanding of Phase II–III drug development and contributions to drug development strategies.

Responsibilities

• Support the development and implementation of the Clinical Development Plan (CDP) for assigned molecule(s)/indication(s).
• Collaborate with internal and external partners across multidisciplinary teams.
• Participate in meetings and reviews for early development/Phase I to provide clinical input.
• Contribute to regulatory filings and regulatory documentation with CST and stakeholders.
• Ensure CDP alignment with CD strategy and develop CDP components (analytics, publications, etc.).
• Lead or contribute to regulatory submissions and related processes.

Skills

Clinical trial experience

Medical monitoring

Data analysis

Scientific writing

Communication skills

Team collaboration

Education

MD/PhD in Oncology & Hematology

Job description

Genentech is seeking a Lead Medical Director for on-site roles in Boston, MA, responsible for shaping the Clinical Development Plan (CDP) for assigned molecules and ensuring alignment with overall strategy. You will collaborate with cross-functional teams, provide clinical input for early development and Phase II/III protocols, and contribute to regulatory submissions.

The role requires MD/PhD with oncology/hematology focus, 5+ years of clinical/research experience, and 3+ years in late-stage