
51 - 200 employees
Founded 2013
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $217M Post-IPO Equity on 2020-08
Healthcare • Biotechnology • Pharmaceuticals
Adverum Biotechnologies is a company focused on developing gene therapies to treat debilitating ocular diseases. Their mission is to establish gene therapy as a new standard of care, particularly in treating conditions like wet age-related macular degeneration (wet AMD), which is a leading cause of blindness globally. The company is advancing their investigational gene therapy Ixo-vec, designed to provide a long-lasting treatment through a single in-office administration, which could replace the current standard of frequent and painful eye injections. By leveraging their proprietary adeno-associated virus (AAV) vector platform, Adverum aims to transform the standard of care, improve accessibility to treatment, and achieve significant societal impact by restoring vision and preventing blindness.
🔥 2 hours ago
🏄 California – Remote
💵 $65 - $110 / hour
⏳ Contract/Temporary
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
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51 - 200 employees
Founded 2013
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
💰 $217M Post-IPO Equity on 2020-08
Healthcare • Biotechnology • Pharmaceuticals
Adverum Biotechnologies is a company focused on developing gene therapies to treat debilitating ocular diseases. Their mission is to establish gene therapy as a new standard of care, particularly in treating conditions like wet age-related macular degeneration (wet AMD), which is a leading cause of blindness globally. The company is advancing their investigational gene therapy Ixo-vec, designed to provide a long-lasting treatment through a single in-office administration, which could replace the current standard of frequent and painful eye injections. By leveraging their proprietary adeno-associated virus (AAV) vector platform, Adverum aims to transform the standard of care, improve accessibility to treatment, and achieve significant societal impact by restoring vision and preventing blindness.
• Drive quality control and endorsement of scientific communication platforms, lexicons, disease-state education materials, program slides, data/publication updates, and congress materials • Serve as a key scientific lead, providing editorial, scientific, and strategic expertise for assigned projects • Lead research-focused data analysis and interpretation of clinical trial data for future podium presentations and publications • Develop and implement strategic publication plans with cross-functional therapeutic-area teams, internal authors, R&D clinical leads, and study statisticians • Review and assist with medical writing for scientific communications and manage external vendors • Oversee the review, preparation, and delivery of high-quality publications, presentations, and abstracts • Review project-related content for accuracy and consistency • Support Field Medical, attend conferences, cover scientific sessions and booths, and serve as a scientific expert with external stakeholders, KOLs, and healthcare professionals • Contribute to innovative communications using interactive PDFs, infographics, podcasts, and novel digital media • Facilitate dissemination discussions for published data and contribute to strategic scientific communications plans and platforms • Lead projects and deliver documents within process and timeline constraints • Support scientific communication and medical affairs activities across clinical trial, pre-launch, and launch stages
• Terminal degree required (PharmD, PhD, MD, or equivalent) • Ophthalmology or gene therapy experience highly desired • Minimum of two years of publication experience is preferred • 5–7 years of industry experience • Demonstrated experience effectively presenting clinical/scientific information required • Ability to learn other disease states if necessary • Excellent communication and presentation skills required • Demonstrated ability to build productive collaborations with medical experts • Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware required • Ability to interface effectively with Clinical Development, Clinical Operations, Translational Research, Technical Operations, Medical Affairs, and the Office of the Chief Medical Officer • Willingness to travel to company meetings and medical congresses • Excellent time management and ability to work independently • Ability to thrive both as part of a team and independently • Well organized, polished, proactive, detail-oriented, mature, and professional demeanor
• Hourly compensation of $65.00 USD to $110.00 USD per hour • Compensation and benefit options provided by the vendor in accordance with specific state requirements • Paid sick leave accrual • Opportunity to contribute to meaningful work within gene therapy and ophthalmology care
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