Associate Director, Global Intake and Triage Leader

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.Purpose:The Associate Director / Director, Global Intake and Triage Leader provides operational leadership for the end-to-end intake and triage processes for all Individual Case Safety Reports (ICSRs) across global Lilly and vendor operations. This role ensures timely, accurate, and compliant receipt, acknowledgment, and initial assessment of adverse event information from all sources globally. This role reports to the Sr. Director / Executive Director, Case Management Operations.Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any role/position can change over time and can include additional responsibilities not specifically described in the job description. Collaborate with your supervisor regarding your actual job responsibilities and any related duties that might be required for the role/position.Operational Leadership - Intake and TriageLead global operations for case intake from all sources including spontaneous reports, clinical trials, literature, digital/social media, regulatory authorities, business partners, and patients/consumersOversee global triage processes ensuring accurate case classification, prioritization, and routing based on regulatory timelines and medical urgencyManage acknowledgment of receipt processes ensuring compliance with regulatory time frames (24-hour acknowledgment where required)Lead invalid case assessment and follow-up activities to obtain minimum criteria for valid ICSRsOversee literature screening and case identification processes across all monitored publicationsEnsure appropriate issue pathways for serious, unexpected, or urgent safety issuesEnsure regulatory compliance with FDA, EMA, ICH, and other health authority requirements for case receipt and initial processingMaintain oversight of intake performance metrics including receipt acknowledgment timeliness, triage accuracy, and intake quality scoresImplement improvement initiatives to optimize intake efficiency and reduce processing timeSupport internal and external regulatory inspections and audits through direct involvement, resource coordination, document preparation, and subject matter expertise.Cross-Functional CollaborationPartner with Medical Information, Affiliates, Medical Affairs, and Regulatory teams to ensure seamless case receipt workflowsCollaborate with Case Processing and Reporting leaders to ensure smooth handoffs and clear communicationCommunicate with Technology teams to optimize case management system functionality for intake processesSupport Product Quality/Complaint Management integration for combination product adverse eventsCollaborate with Case Management Commercial and Clinical Liaison to ensure seamless flow of information from various programs such as PSP, Market Research, etc.People Management and Development Supervise multiple Manager-level leaders and their teams across global operations sites with dynamic prioritization based on volume and complexity.Translate departmental strategic plans into operational objectives and ensure team execution of adverse event collection standards across clinical trials and commercial programs.Monitor team performance, provide regular feedback, conduct performance evaluations, and identify development opportunities for direct reports.Foster a collaborative, inclusive team culture that promotes technical excellence, continuous learning, and cross-functional partnership.Ensure team compliance with relevant SOPs, global and local regulations, and training requirements.Understand and Support of the EU QPPV role   Understanding the roles and responsibilities of the EU Qualified Person.   Ensure support is provided to enable the Qualified Person to fulfill all the Qualified Person legal responsibilities.Minimum Qualification Requirements:Bachelor's degree in nursing, pharmacy, life sciences, or related health sciences field5 + years of experience in Pharmacovigilance, with at least 3 years focused on case intake/triage operations2+ years managing people or leading teamsExperience with safety databases (Argus, ARISg, Veeva or similar).Onsite Indianapolis IN, (3 days onsite / 2 remote)Other Information/Additional Preferences:Experience managing vendor relationships and outsourced operationsStrong understanding of global pharmacovigilance regulations (FDA, EMA, ICH guidelines) and Good Pharmacovigilance Practices (GVP) and ICSR processing requirementsKnowledge of literature monitoring and digital/social media surveillanceStrong analytical skills with experience in metrics-driven operationsExcellent communication skills in English (verbal and written)Ability to work effectively in a matrix, multicultural global environmentAbility to travel when requiredLilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender exp