Head of Therapeutics
Company | Earli, Inc. |
---|---|
Location | San Carlos, CA, USA |
Salary | $Not Provided – $Not Provided |
Type | Full-Time |
Degrees | PhD |
Experience Level | Expert or higher |
Requirements
- PhD or advanced degree in Biochemistry, Cell Biology, Molecular Biology, or a related discipline.
- Minimum of 10+ years of firsthand industry experience in developing cancer therapeutics using engineered proteins delivered via gene therapy approaches including ‘first in class’ products as well as ‘best in class’ products
- 8+ years direct experience building, inspiring, and managing high-performing multidisciplinary teams in biopharma
- Strategic thinker with deep expertise in advancing novel gene therapy drugs with a track record of having taken one or more drugs from white board to IND and clinical studies
- Deep expertise in immuno-oncology drug development is strongly preferred
- Strong track record of scientific productivity as evidenced by high-quality, impactful publications
- Thrive in a collaborative team setting and be driven to be innovative in a high energy, small company environment
- Ability to handle multiple workflows simultaneously and meet aggressive project timelines
Responsibilities
- Lead the Earli Therapeutics Team to develop and advance novel non-viral gene therapy approaches using the Earli platform for the treatment of cancer.
- Drive high-level strategy to down-select specific candidates for clinical development and generate appropriate efficacy and safety data packages for regulatory submission
- Ensure that innovation is coupled with scientific rigor to drive program development strategies
- Work with cross functional team leads (Gene Regulation, Delivery, Translational Biology) to create and execute on research roadmap for clear no-go/go decisions under expedited timelines
- Act as the primary stakeholder to drive and communicate milestones and timelines to other senior leaders within the company as well as to external collaborators and advisors
- Inspire, develop and empower the therapeutics team as well as provide technical expertise/scientific guidance
- Write technical sections for IND and other regulatory filings
- Work with the Head of BD and CSO to establish external partnerships with key pharma collaborators and academic labs
- Work with the CSO and SAB members/KOLs to develop Target Product Profiles (TPPs) for lead therapeutic programs and ensure alignment of pre-clinical development strategy with TPP
Preferred Qualifications
- Deep expertise in immuno-oncology drug development is strongly preferred