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Sr. Medical Director

4D Molecular Therapeutics
Full-time
Remote friendly (United States)
United States
$315,000 - $390,000 USD yearly
Clinical Research and Development

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Role Summary

The Senior Medical Director is accountable for the design, execution, and analysis of clinical trials in the Ophthalmology Therapeutic Area.

Responsibilities

  • Provides clinical leadership to multidisciplinary study execution teams drawn from clinical operations, clinical science, biometrics, regulatory affairs, CMC, pharm/tox, drug safety, commercial, and alliance partners
  • Has lead accountability on the study teams for delivery of study protocols, study conduct, and study readouts
  • Organizes and leads scientific advisory board meetings. Interacts with external experts and stakeholders to gather input
  • Serves as medical monitor on clinical studies
  • Serves as the primary clinical author of development plans, study protocols, amendments, ICFs, IBs, INDs, annual reports, CSRs, regulatory submissions / correspondence, and project-related documents. Accountable for the accuracy of all medical content of such documents
  • Works with the research organization and the portfolio management team to identify and support new project opportunities
  • Collaborates to identify program risks, and to create and implement mitigation strategies
  • Other duties as assigned

Qualifications

  • Medical Degree (M.D.)
  • Residency training in Ophthalmology with a preference for subspecialty training in retina
  • Board certification a plus
  • Retina fellowship training a plus
  • 8+ years of clinical ophthalmology research in the biopharmaceutical industry
  • Experience with Phase 3 retina clinical trials
  • Experience with gene therapy a plus
  • Experience in other phases (Phase 1, 2, 4) of clinical research a plus
  • Experience with NDA/BLA/MAA submission a plus
  • Experience writing clinical research protocols and acting as a medical monitor
  • Experience in data analysis, data interpretation, and medical writing

Skills

  • Knowledge of ICH-GCP and FDA regulatory guidelines
  • Knowledge of international regulatory guidelines a plus
  • Effective written and verbal communication skills, including public speaking

Education

  • Medical Degree (M.D.)
  • Residency training in Ophthalmology with a preference for subspecialty training in retina
  • Board certification a plus
  • Retina fellowship training a plus

Additional Requirements

  • Travel: 15% (3 days/month)
  • Physical Requirements and Working Conditions:
    • Physical Activity - Repetitive motions: Making substantial movements of the wrists, hands, and/or fingers; Fingering; Talking
    • Physical Requirements - Sedentary work: Exerting up to 10 pounds of force occasionally; mostly sedentary
    • Working Conditions - The worker is not substantially exposed to adverse environmental conditions
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