Medical Director

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November 13

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4D Molecular Therapeutics

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4DMT is a clinical stage biopharma company inventing and developing innovative products to unlock the full potential of genetic medicine to treat large market and rare diseases. Our vector discovery platform Therapeutic Vector Evolution harnesses the power of directed evolution, a Nobel Prize-winning technology, with approximately one billion synthetic AAV capsid-derived sequences to invent customized and evolved vectors with improved therapeutic profiles compared to wild-type vectors. Our product design, development and manufacturing engine empowers us to efficiently create our valuable and diverse product pipeline. This combination of bold innovation and relentless execution gives 4DMT the capability to revolutionize genetic medicines and to strive for potential curative therapies. We have built a deep portfolio of genetic medicine product candidates, with five product candidates in clinical trials for seven patient populations.

51 - 200 employees

📋 Description

• Act as medical monitor in clinical ophthalmology studies with a focus on safety, data review and analysis of emerging data • Contribute to study related documents including but not limited to study synopsis, protocols, amendments, ICFs, IBs, INDs, annual reports, CSRs, and other regulatory submissions and project-related documents. Accountable for the medical content of documents. • Analyze, interpret, and organize data for presentations and publications • Interact with external experts to gather input. Organize scientific advisory board meetings and data safety monitoring committee meetings • Maintain a high level of clinical and scientific expertise in ophthalmologic disease area(s) by reviewing the literature and attending medical/scientific meetings • Ability to communicate with Investigators and research site staff to ensure rigorous and compliant study conduct • Able and willing to travel

🎯 Requirements

• Medical Degree (M.D.) with clinical experience • Clinical residency training in ophthalmology required. • Experience with retinal disease, retinal imaging, or gene therapy • 5+ years of experience in clinical research in the pharmaceutical/biotech industry • Experience writing clinical research protocols and acting as a medical monitor preferred • 4 yrs Phase III clinical research experience required • Effective written and verbal communication skills • Knowledge of ICH-GCP and FDA regulatory guidelines

🏖️ Benefits

• Equal employment opportunities for all employees and applicants