Senior Vice President of Clinical Ophthalmology

2 weeks ago


California, United States Partnology Full time

A well-capitalized biotechnology firm is in search of an experienced ophthalmologist to lead the clinical development efforts in their ophthalmology division. This role will involve close collaboration with the Chief Medical Officer to spearhead the primary initiative focused on Retinitis Pigmentosa, as well as strategizing and implementing subsequent programs.

Key Responsibilities:

  • Oversee the formulation of study protocols, execution of clinical trials, and analysis of study outcomes, ensuring the successful delivery of clinical programs.
  • Manage cross-functional clinical teams, including clinical operations, clinical science, biostatistics, regulatory affairs, CMC, pharmacology/toxicology, drug safety, commercial strategy, and external partners.
  • Engage with external specialists and advisory panels to obtain valuable insights.
  • Collaborate with central testing facilities to influence the development of clinical endpoints and enhance patient assessment methodologies.
  • Contribute to the drafting of study protocols, amendments, informed consent forms, investigator brochures, IND applications, annual reports, clinical study reports, and other regulatory documents, ensuring the medical accuracy of all content.
  • Lead and support the preparation of clinical research grant proposals.
  • Work in partnership with the research division to discover and promote new project opportunities within ophthalmology and other therapeutic fields.
  • Identify potential program risks and develop strategies for mitigation.

Desired Skills and Experience:

  • Medical Degree (M.D.) is required.
  • Board certification in ophthalmology is highly preferred.
  • Experience across various phases of clinical research (Phase 1-3) is preferred.
  • Familiarity with retinal diseases, imaging techniques, psychophysics, or gene therapy is advantageous.
  • A minimum of ten (10) years of clinical research experience within the pharmaceutical or biotechnology sector is essential.
  • In-depth understanding of clinical regulatory frameworks (US FDA, EMA, etc.) and ICH-GCP guidelines is preferred.
  • Proven experience in authoring and presenting clinical research findings is strongly preferred.
  • Exceptional written and verbal communication skills are necessary.
  • Experience in leading multidisciplinary teams is required.


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