
201 - 500 funcionários
Fundada em 2019
🏥 Saúde
💼 Consultoria
🏭 Manufatura
💰 $150.000.000 Series D - Enveda Biosciences em 2025-09
Healthcare • Consulting • Manufacturing
A Enveda é uma empresa de biotecnologia que utiliza uma plataforma proprietária para decodificar e traduzir a diversidade química da natureza, acelerando a descoberta de fármacos de pequenas moléculas. Ao purificar, identificar e caracterizar rapidamente moléculas de fontes naturais complexas, a Enveda pretende colocar um vasto espaço químico, derivado evolutivamente, nas mãos dos exploradores de medicamentos para descobrir tratamentos mais rapidamente e expandir o pipeline de terapêuticos.
🕒 Ontem
🇺🇸 Estados Unidos – Remoto (EUA)
💵 $225.000 - $250.000 / ano
⏰ Tempo Integral
🔴 Especialista
👔 Diretor
🦅 Patrocina Visto H1B
👻 Score fantasma 0%
🗣️🇺🇸🇬🇧 Inglês obrigatório
De onde vem esta vaga
Publicada na página de carreiras da Enveda, não em um site de vagas
Vista pela primeira vez pelo Remote Rocketship Ontem
Ainda aberta no site da Enveda. Verificada 26 minutos atrás.

201 - 500 funcionários
Fundada em 2019
🏥 Saúde
💼 Consultoria
🏭 Manufatura
💰 $150.000.000 Series D - Enveda Biosciences em 2025-09
Healthcare • Consulting • Manufacturing
A Enveda é uma empresa de biotecnologia que utiliza uma plataforma proprietária para decodificar e traduzir a diversidade química da natureza, acelerando a descoberta de fármacos de pequenas moléculas. Ao purificar, identificar e caracterizar rapidamente moléculas de fontes naturais complexas, a Enveda pretende colocar um vasto espaço químico, derivado evolutivamente, nas mãos dos exploradores de medicamentos para descobrir tratamentos mais rapidamente e expandir o pipeline de terapêuticos.
• Own studies end to end as clinical lead, from protocol through start-up and enrollment • Write protocols and clinical sections of regulatory documents, making study-level design decisions and presenting endpoint, population, and go/no-go recommendations to the Global Program Head • Work with Clinical Operations to hold CROs, sites, and vendors accountable for timelines, enrollment, budget, and data quality • Review blinded safety, PK, and operational data with the medical monitor and act on findings • Work flexibly across decisions and therapeutic indications • Take on studies in additional indications as pipeline needs require • Use AI in daily work to support and improve ways of working, and share effective practices with the team • Build relationships with investigators, sites, and KOLs • Bring the patient's perspective into consequential decisions • Report to the SVP of Clinical Development and collaborate with Global Program Heads, Clinical Operations, and medical monitors
• An advanced degree (MD, DO, PhD, PharmD, or equivalent) • Hands-on clinical development experience: written protocols as primary author and taken at least one study from protocol to database lock as its lead • Typically 8+ years for a clinical scientist, or 3+ years in industry after clinical training for a physician • Clinical or trial experience in inflammatory bowel disease, ideally with endoscopic endpoints and central reading (preferred, not required) • Experience in a second therapeutic area • Data-driven judgment using clinical, safety, and operational data to make decisions • Ability or willingness to use AI to draft, check, and interrogate work, with awareness of where it can mislead • Collaborative, direct, high-agency, patient-first approach
• Medical, dental, and vision covered at 90% • 401(k) with company match • Flexible PTO • Company-wide weeklong recharge break • Adoption assistance
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