Associate Scientist, Clinical Development

Role: Clinical scientist supporting early and late-phase clinical development, with responsibilities in study design, execution oversight, data management, and analysis. Contributes to multidisciplinary teams by integrating medical, scientific, regulatory, and commercial insights to optimize clinical trial methodology and outcome measures. May lead program discussions and data presentations internally and externally. Requirements: BA/BS or MA in Data Sciences, Psychology, or related field; 2+ years industry experience; strong knowledge of regulatory practices, GxP, and clinical trial processes. High-Value: Involvement in neuroscience/neurology indications, supporting clinical trials from early to late phases, with focus on outcome measure development, protocol design, and regulatory documentation support. Collaboration with external opinion leaders, internal clinicians, and cross-functional teams. WorkSetup: Not specified, but involves clinical data review, study support, and regulatory interactions.