Associate Director, Clinical Scientist

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 PhD or equivalent degree with 2+ years of relevant experience, or bachelor’s/master’s degree with 5+ years of relevant post-graduate experience, including pharmaceutical industry experience in clinical drug or biologics development. Experience as a Clinical Scientist or in a comparable clinical development role with the ability to work independently. Hands-on experience reviewing, analyzing, and interpreting clinical trial data. Strong cross-functional collaboration, organizational, communication, and presentation skills. Preferred Capabilities: Experience supporting Phase I-III clinical development programs. Clinical development experience in oncology and/or neurology. Rare disease experience. Flexible hybrid or remote work arrangement within approved U.S. working locations. Up to...

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