
51 - 200 employees
Founded 2015
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Neurelis, Inc. is a neuroscience-based company dedicated to developing innovative treatments for people living with neurological conditions. With a focus on enhancing therapeutic benefits and addressing unmet needs in care, Neurelis is committed to empowering individuals to define their own journey. The company boasts a range of proprietary non-invasive drug delivery technologies, including Intravail, ProTek, and Hydrogel, which enhance drug development and clinical performance. Neurelis's pipeline includes several FDA-approved treatments and investigational product candidates at various stages of development. Neurelis is also involved in community activities and offers saving and support programs to ensure accessibility of their therapies.
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51 - 200 employees
Founded 2015
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Neurelis, Inc. is a neuroscience-based company dedicated to developing innovative treatments for people living with neurological conditions. With a focus on enhancing therapeutic benefits and addressing unmet needs in care, Neurelis is committed to empowering individuals to define their own journey. The company boasts a range of proprietary non-invasive drug delivery technologies, including Intravail, ProTek, and Hydrogel, which enhance drug development and clinical performance. Neurelis's pipeline includes several FDA-approved treatments and investigational product candidates at various stages of development. Neurelis is also involved in community activities and offers saving and support programs to ensure accessibility of their therapies.
• Oversee Scientific Operations activities and programs, including strategic annual planning. • Manage the budget, including tracking, analyzing, and reporting quarterly budget-to-forecast variances. • Provide strategic guidance on Medical, Legal, and Regulatory (MLR) review processes. • Manage the publication vendor in the development and execution of strategic publications. • Ensure compliance with all applicable guidelines and regulations, including Fair Market Value (FMV) requirements and Sunshine Act reporting. • Partner closely to ensure appropriate resources are deployed to support clinical development studies.
• Bachelor’s degree with 10+ years of relevant experience, Master’s degree with 8+ years of relevant experience, or PhD with 6+ years of relevant experience preferred. • Demonstrated experience in Clinical Development and Medical Affairs functions within the biopharmaceutical industry required.
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