Heme, Research Fellow

Scorpion Therapeutics

Boston (MA)

On-site

USD 350,000 - 550,000

Full time

7 days ago
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Job summary

Scorpion Therapeutics seeks a senior leader to drive lead discovery and translational research for in vivo gene editing therapies targeting hemoglobinopathies. The role spans target selection, preclinical work, IND-enabling studies, and Phase 1/2 trial readiness.

Responsibilities include shaping scientific strategy, guiding in vitro/ex vivo/in vivo studies, supporting candidate optimization, and leading cross-functional teams toward nomination of a development candidate.

Qualifications

  • MD or PhD with 11+ years in biotech/pharma research and drug development.
  • Expertise in translational science and disease biology.
  • Experience with cell/gene therapy and genome editing.

Responsibilities

  • Lead in vivo gene editing programs for hemoglobinopathies.
  • Direct target selection, preclinical, IND-enabling studies, and early clinical planning.
  • Guide cross-functional teams to nominate development candidates and shape strategy.

Skills

Drug development
Translational science
Disease biology
Cell therapy
Genome editing
GMP/GLP knowledge

Education

MD/PhD

Job description

Role

Lead drug discovery and translational research for in vivo gene editing therapies targeting hemoglobinopathies, with responsibilities spanning target selection, preclinical, IND-enabling studies, and Phase 1/2 trials. Responsibilities include shaping scientific strategy, guiding in vitro/ex vivo/in vivo studies, supporting target and candidate optimization, and leading cross-functional teams toward development candidate nomination.

Requirements
  • MD and/or PhD with 11+ years in academic, biotech, or pharma research, expertise in drug development, translational science, and disease biology, with experience in cell/gene therapy and genome editing.
Preferred
  • Direct hemoglobinopathy experience (e.g., sickle cell, thalassemia), familiarity with delivery systems, editing efficiency, HSC biology, regulatory pathways (FDA/EMA), and GCP.
High-Value
  • Hemoglobinopathies, gene editing, in vivo pharmacology, IND-enabling programs, clinical translation, and leadership in matrixed environments.
Work setup

On-site, five days/week, with ad hoc flexibility.

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