Lead Scientist - In Vivo Genome Editing for Personalized Therapies

St. Jude Children's Research Hospital

Memphis (TN)

On-site

USD 126,000 - 238,000

Full time

14 days+

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Job summary

St. Jude Children's Research Hospital seeks a Lead Scientist to guide the development of an in vivo base editing platform for pediatric patients with bone marrow disorders.

You will lead efforts in genome editing drug development, IND-enabling studies, and translation to clinical trials with room for growth. The role requires a PhD with extensive experience in genomics and CRISPR, and a track record of managing multidisciplinary teams in a fast-paced research lab environment.

Qualifications

  • PhD in relevant scientific area is required, such as genomics, molecular and cell biology.
  • Expertise in genome editing, genomics, next-generation sequencing.
  • Excellent communication, organizational, and presentation skills.
  • Four or more years of hands-on research laboratory experience working with CRISPR genome editors and NGS library preparation.

Responsibilities

  • Coordinate a team of scientists to develop a novel gene editing platform.
  • Accelerate lead-target discovery, genotoxicity characterization, and cargo optimization.
  • Conduct non-clinical pharmacology studies of an HSC-targeted lipid nanoparticle.
  • Continuously assess and manage project technical and drug development risks.
  • Analyze experimental outcomes and develop high-quality summaries.
  • Summarize results and present updates to DRIVE and ARPA-H teams.
  • Draft manuscripts and figures for publication in high-impact journals.

Skills

Genomics
Genome editing
NGS library prep
CRISPR editors
Data interpretation
Team leadership

Education

PhD in genomics/molecular/cell biology
Master’s degree in relevant field
Bachelor’s degree in related field

Job description

St. Jude Children's Research Hospital seeks a Lead Scientist to guide the development of an in vivo base editing platform for pediatric patients with bone marrow disorders.

You will lead efforts in genome editing drug development, IND-enabling studies, and translation to clinical trials with room for growth. The role requires a PhD with extensive experience in genomics and CRISPR, and a track record of managing multidisciplinary teams in a fast-paced research lab environment.

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