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Head of Therapeutics

Head of Therapeutics

CompanyEarli, Inc.
LocationSan Carlos, CA, USA
Salary$Not Provided – $Not Provided
TypeFull-Time
DegreesPhD
Experience LevelExpert 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