Responsibilities

As a Trial Activation Feasibility Specialist II, the individual will collaborate closely with local clinical operations management and the Feasibility Manager, initiating feasibility intelligence collection, vetting local site lists, identifying risks to quality and compliance, maintaining investigator and site staff contact details, documenting communication attempts, managing primary investigator changes, reviewing DPA/ISD status, supporting survey data review, achieving targeted response goals, serving as a local guide on site capacity, championing strategic site inclusion, conducting phone interviews, conducting on-site visits, collecting data on site capabilities, and providing local knowledge for site development.