Clinical Scientist Associate Director

Key Responsibilities: Lead ongoing clinical data review to ensure data quality and patient safety Contribute to the development and review of clinical documents such as study protocols and regulatory submissions Represent Clinical Development on cross-functional study teams and prepare clinical data presentations for various stakeholders

Required Qualifications: PhD or equivalent degree with 2+ years of relevant experience, or bachelor's/master's degree with 5+ years of relevant post-graduate experience in clinical drug or biologics development Experience as a Clinical Scientist or in a comparable clinical development role Hands-on experience in reviewing and interpreting clinical trial data Strong cross-functional collaboration and organizational skills Experience supporting Phase I-III clinical development programs, preferably in oncology or neurology