Clinical Scientist

• Contributes to clinical and pre-clinical program development strategy and execution
• Analyzes and interprets study data, and prepares scientific reports and presentations
• Contributes to and authors strategic documents including pre-clinical and clinical sections of regulatory documents such as Investigator’s Brochures, IND submission documents, study protocols, statistical analysis plans, responses to Health Authority questions
• Contributes to study-related advisory boards and investigators’ meetings
• Manages collaborations with external groups
• Leads translational special interest
• Contributes to the development of abstracts, presentations, and manuscripts
• Assists with design, development and implementation of training programs for more junior colleagues
• Assists with clinical site evaluation