The Associate Director, Clinical Scientist plays a key role in the execution of clinical development programs, partnering with Medical Directors and cross-functional study teams to support clinical data review, interpretation, study documentation, and communication of findings. This is a hands-on role for an experienced Clinical Scientist who can work independently, identify and escalate meaningful clinical findings, and collaborate effectively across Clinical Operations, Data Management, Biostatistics, Pharmacovigilance, Regulatory, and other functions. Key Responsibilities: Clinical Data Review & Study Execution Lead ongoing clinical data review to support data quality, interpretation, and patient safety. Identify and escalate clinically relevant findings and partner with study teams to resolve data-related issues. Collaborate with Data Management and Clinical Operations on study implementation and EDC development. Clinical Documents & Data Outputs Contribute to the development and review of clinical documents, including study protocols, investigator brochures, regulatory documents, concept materials, and other study-related documentation. Review and interpret clinical study data and outputs in partnership with Biostatistics, Pharmacovigilance, and other stakeholders. Cross-Functional & Scientific Leadership Represent Clinical Development on cross-functional study teams and work closely with Medical Directors and other functional partners. Prepare and present clinical data, study designs, and scientific information for study teams, investigator meetings, advisory boards, study committees, and other internal or external audiences. Other duties and responsibilities as assigned 
