Associate Director – CTF Clinical Results Systems

Company: Eli Lilly and Company
Location: Indianapolis
Posted on: June 25, 2025

Job Description:

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, CTF Clinical Results Systems (as part of Clinical Trial Foundations) is a leader and key partner across the business. They will serve as the point to manage the technologies and processes to support information flow and process automation within their teams. They will provide coaching and consultation on the following: technologies, standards, vendor management, inspection readiness, data flow knowledge, and shared learnings. They will also provide first line supervision to a team of individuals. 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 position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. 1. People Management ? Recruit, retain, develop, and leverage the very best talent available, internally and externally, to meet technical, scientific, and strategic needs ? Assign, coach and develop staff such that they provide consistent, positive, strong technical leadership to the entire organization ? Create an environment where staff feel comfortable speaking up so that a broad range of ideas and thoughts are vetted and explored; where they are fully engaged in our work so that their passion is fully engaged; and where roles and responsibilities are optimized to the individual so that the full range of their talents are brought to bear on critical and meaningful work 2. Operational Management ? Prioritize work based on strategy and communicate and coordinate resulting decisions with crossfunctional leaders ? Build and leverage relationships with Process Owners, Leadership, clinical development, quality, and IT in order to ensure understanding, agreement and alignment on systems and accompanying business processes ? Partner with Third Parties to ensure high quality, on-time, on budget deliverables along with constant implementation of process improvements and efficiencies ? Monitor relevant performance metrics and implement actions as needed ? Manage budget and reporting activities ? Maintain inspection readiness ? Work with Lilly quality organizations to ensure support for vendor qualifications, audits, and inspections 3. Technology and Process Management ? Approach new and existing work by assessing and articulating quality and business requirements for the technologies we own ? Understand business strategies, processes and technology as it relates to clinical development ? Work to develop best practices, process improvements specifically in the Coding area ? Execute and maintain the clinical information management and process automation strategy for their area of focus in partnership with business and IT partners ? Accountable for understanding and managing Coding for clinical trials Minimum Qualification Requirements: ? Experience with Coding ? Familiarity with WHODrug and MedDRA ? Bachelor’s degree or equivalent experience ? Experience leading large-scale programs and/or initiatives ? In depth knowledge of data standards, the clinical data flow, and the supporting technology ? Ability to work in a virtual team environment, with outsourced partners ? Strong oral and written communication skills ? Demonstrated ability to build and foster teamwork, and strong ability to work across functions and regions ? Ability to provide on-going feedback, coaching, and direction ? Ability to positively manage and resolve conflict ? Demonstrated leadership and influence skills ? Demonstrated interpersonal and relationship building skills ? Demonstrated ability to deliver to timelines ? Ability to focus on multiple, competing priorities and customers simultaneously ? Critical thinking skills ? Ability to adjust rapidly to unexpected business opportunities (flexibility) ? Ability to proactively identify potential issues and contingency plans. Other Information/Additional Preferences: ? Knowledge of and experience with discipline-related processes and technology ? Knowledge of emerging IT capabilities used for clinical trial data management ? Capacity and workload management expertise ? Strong leadership skills ? Outstanding interpersonal skills ? Demonstrated ability to influence and motivate ? Excellent oral and written communication skills ? Ability to positively manage and resolve conflict ? Strong focus on customer and business results ? Demonstrated ability to build and foster teamwork ? Strong ability to work across functions and regions ? Demonstrated ability to deliver on-time performance ? Ability to provide on-going feedback, coaching, and direction Lilly 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 expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $118,500 - $173,800 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. WeAreLilly

Keywords: Eli Lilly and Company, Lawrence , Associate Director – CTF Clinical Results Systems, Science, Research & Development , Indianapolis, Indiana