Director, Medical Information

🕒 June 25

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Neurelis, Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2015

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

Healthcare • Manufacturing • Biotechnology

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.

📋 Description

• Supports Neurelis’ Medical Information function by leading the development and maintenance of core medical content • Provides product and disease-state training to internal stakeholders and vendors • Serves as a subject matter expert for internal and external audiences • Reviews and approves medical materials that are scientifically accurate and clinically relevant through the Medical/Legal/Regulatory (MLR) compliance process • Supports Publication Response Team activities and provides scientific presentations and evidence-based responses to payors in support of Market Access • Contributes to cross-functional Medical Affairs initiatives • Applies scientific expertise to address escalated product and disease-state inquiries • Develops quarterly internal newsletters • Maintains AMCP dossier updates and provides scientific input on company products • Supports vendor training activities and contributes to the oversight of Medical Information quality and operational performance.

🎯 Requirements

• Advanced degree in life sciences (PharmD, PhD, MD, NP) • 6+ years of experience in the industry, with the majority spent within Medical Affairs • Experience serving as a Medical reviewer within Medical, Legal, and Regulatory (MLR) review process • Working knowledge of Medical Information creation and delivery, including the ability to evaluate information from multiple sources • Experience in conducting literature searches, evaluating literature, and applying drug information concepts • Knowledge and understanding of medical terminology, drug names/classes, clinical and pharmaceutical aspects of medicines • Strong analytical and problem-solving skills.