We’re looking for people who are determined to make life better for people around the world.

Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for a site’s ERB and Competent Authority (CA)(where applicable), communicate and negotiate budgets with site personnel and internal teams, negotiate and obtain fully-executed contract, track and ensure site compliance to required training, and effectively drive timelines aligned with company priorities Communicate with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out Communicate with various internal and external party / clinical research organization to enable active collaboration during site activation, maintenance and close-out Site budget/contract development and management Manage investigator payments and any other financial transactions Identify, communicate, and resolve issues Coordinate the management and delivery of clinical trial material Coordinate translation process for clinical trial documents and oversight of translation quality Populate internal systems to ensure accuracy of trial / site performance Populate Trial Master Files and libraries for future reference Inspection readiness of regulatory documents and processes Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#We Are Lilly