Trial Capabilities Associate, Italian

<p>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 employees around the world 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.</p><p></p><p><span><span><span>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 around the world 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 patients around the world. </span><br/><br/><span>Eli Lilly Cork, is made up of a talented diverse team of over 1,400 employees across 38 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more.</span></span></span></p><p><span><span><span>Lilly offers a premium workspace across our campus in Little Island,  complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking.  Inhouse People Development services, Educational Assistance, and our ‘Live Your BEST Life’ wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.</span><br/><br/><span>Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself!</span></span></span></p><p><span><span> </span></span></p><p><span><span><span><b>Job description</b></span></span></span></p><p><span><span><span>The Trial Capabilities Team provides clinical trial capabilities in support of clinical development.  The Associate is accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and <span>closeout.  </span> The Associate is responsible for obtaining clinical trial authorizations and ethical <span>approvals, execution</span> of the budget and contract, and activities related to clinical finance, records management and site <span>training.  </span></span></span></span></p><p><span><span> </span></span></p><p><span><span><span>The Associate will ensure inspection readiness through a complete, accurate and readily available Trial Master File.  Additional local responsibilities may be required as needed/appropriate for the local geography and/or to cover regional <span>differences.  </span></span></span></span></p><p><span><span> </span></span></p><p><span><span><span><b>Key Objectives / Deliverables:</b></span></span></span></p><p><span><span> </span></span></p><p><span><span><span><b>Clinical Trial Capabilities Responsibilities</b></span></span></span></p><ul><li><span><span><span>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</span></span></span></li><li><span><span><span>Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out</span></span></span></li><li><span><span><span>Identify, communicate, and resolve issues</span></span></span></li><li><span><span><span>Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems</span></span></span></li><li><span><span><span>Leverage previous site / review board engagements to efficiently drive new work</span></span></span></li><li><span><span><span>Populate internal systems to ensure accuracy of trial / site performance</span></span></span></li><li><span><span><span>Understand and comply with procurements, legal and financial requirements and procedures</span></span></span></li><li><span><span><span>Populate Trial Master Files and libraries for future reference</span></span></span></li><li><span><span><span>Provide feedback and shared learning for continuous improvement</span></span></span></li><li><span><span><span>Leverage tria