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 35,000 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 people around the world.

Organization Overview:

Are you seeking a career that makes a difference in the world? Do you have healthcare informatics expertise? Do you want to apply your clinical support experience in a business setting? Are you good at interpreting and connecting information from a variety of sources? If so, we have the role for you.

The Clinical Design Delivery & Analytics (CDDA), a division of Lilly Research Laboratories, partners with Medical colleagues in Research, Oncology, Immunology, Neuroscience/Pain, and Diabetes to effectively and efficiently design, plan, and implement clinical trials across all phases of research. Uniting experts in clinical development and design, laboratory and data sciences, site engagement, and trial capabilities, the CDDA focuses on participants, patients, and investigators to deliver novel designs and innovative research approaches. Our focus on excellence in bringing these capabilities together and providing diverse career opportunities within global clinical development has established Lilly as an industry leader in bringing new medicines to patients.

The purpose of the Associate Director Informaticist role is to support the design of clinical programs and trials by bringing together internal and external data and information (e.g. contemporary information on standard of care across the globe, understanding of patient pathways that can make trials more accessible within those geographies, etc.), analyses and insights to develop and inform multiple scenarios, driving excellence in clinical trial design, enabling more efficient planning and execution.

Sound interesting to you? Read on to find out the key responsibilities you will have in this role.

1.Develop and communicate scenarios and recommendations for key aspects of clinical program design

• Responsible for delivering and communicating data, information, and insights to support program design decisions in support of the Patient Investigator Country (PIC) business process and related considerations (e.g. scaling of Decentralized Clinical Trials, Value Based Research principles, and enabling Lilly's goals for diverse representation in clinical trials, etc.)
• Responsible for surfacing insights for strategies that can optimize trial and program design for time, value, cost, and/or risk considerations
• Responsible for building plans and scenarios that create accessibility and pathways for participation in Lilly clinical trials as the baseline expectation.
• Partner with the Design Hub Therapeutic Areas to enable insights for study design optimization (e.g. inclusion/exclusion criteria, schedule of events, patient discontinuation, etc.)
• Anticipate and ensure completion of modeling and scenario needs by applying clinical development, TA and modeling expertise

2. Provide Strategic and Technical Leadership for Data Insights capabilities

• Lead the development, release, and adoption of new tools and capabilities among users and consumers for those tools within the Design Hub and broader CDDA community
• Evaluate evolving business partner needs and recommend enhancements to existing tools and capabilities to support emerging opportunities
• Advise leadership on technologies that will assist in expanding informatics capabilities and/or automation/efficiency.
• Support evaluation of new data sources and capabilities that can enhance program and study design decisions
• Provide business user requirements for existing or new technologies and related data sources

Basic Qualifications:

• Bachelor's Degree
• Minimum 5 years experience in the pharmaceutical industry, drug development, and/or related fields

Additional Skills/Preferences:

• Post-graduate degree(s), e.g., Pharm D, M.S.
• Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain expertise to support portfolio needs
• Experience in clinical research or clinical trial planning, design and operations preferred
• Demonstrated experience with implementation of solutions
• Analytical ability to use complex software systems while synthesizing data and information
• Demonstrated experience in navigating ambiguity
• Critical thinking, learning agility, and strategic reasoning also seen as beneficial
• Excellent written and presentation skills

Additional Information:

• Indianapolis based
• 10% or less travel

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( [email protected] ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and 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.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.

As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).

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