Clinical Scientist / Medical Director - Ophthalmic Gene Therapy Biotech

Opus Genetics

Durham (NC)

On-site

USD 180,000 - 280,000

Full time

14 days+

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Job summary

Scorpion Therapeutics seeks a Medical Director / Clinical Scientist to provide scientific and medical leadership for inherited retinal disease (IRD) programs, guiding study design, safety review, and regulatory support.

You will oversee investigator/site engagement, contribute to endpoint definitions and eligibility criteria, and collaborate on regulatory submissions and publications, with hybrid/remote work and East Coast preference.

Qualifications

  • MD/DO or equivalent with clinical development experience.
  • Strong scientific writing skills.
  • Familiar with GCP and regulatory expectations.

Responsibilities

  • Provide scientific and medical leadership for IRD programs.
  • Oversee study design and safety review.
  • Assist with regulatory submissions and publications.
  • Contribute to endpoint and eligibility criteria.
  • Support investigator/site engagement and collaboration.

Skills

Strong scientific writing
GCP familiarity
Clinical development experience

Education

MD/DO or equivalent

Tools

OCT
Microperimetry
Clinical data review

Job description

Role

Medical Director / Clinical Scientist providing scientific and medical leadership for inherited retinal disease (IRD) clinical programs, overseeing study design, safety review, and regulatory support.

Responsibilities
  • develop protocols
  • review safety/efficacy data
  • contribute to endpoint and eligibility criteria
  • support investigator/site engagement
  • collaborate on regulatory submissions and publications
Requirements
  • MD, DO, or equivalent with clinical development experience
  • knowledge of ophthalmology, retinal diseases, or gene therapy preferred
  • experience with OCT, microperimetry, and clinical data review
  • strong scientific writing skills
  • familiar with GCP
High Value
  • IRD (retinal diseases)
  • gene therapy
  • clinical-stage biotech
  • early to pivotal development
  • GCP compliance
  • ophthalmology expertise
  • regulatory interactions
Work Setup

hybrid/remote; East Coast preferred.

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