Clinical Trial Capabilities Responsibilities * 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 directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out * Identify, communicate, and resolve issues * Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems * Leverage previous site / review board engagements to efficiently drive new work * Populate internal systems to ensure accuracy of trial / site performance * Understand and comply with procurements, legal and financial requirements and procedures * Populate Trial Master Files and libraries for future reference * Provide feedback and shared learning for continuous improvement * Leverage trial prioritization * Anticipate and monitor dynamically changing priorities
Internal Number: 50281
About Eli Lilly & Company
Company Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees worldwide work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.