Senior Advisor - Real World Analytics

About Lilly

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.

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Purpose

The Sr. Advisor for Real-World Analytics provides technical leadership and expertise in initiating and carrying out the evidence generation plans for Medical Affairs, Access & Reimbursement, and Real-World Evidence. The Sr. Advisor is responsible for working with scientists to ensure that the proposed evidence generation activities are scientifically sound.

Primary Responsibilities

Statistical Design and Analysis

• Is a successful problem solver who can use technical expertise to work closely with other functions to answer important questions about our products by translating strategic needs into innovative statistical solutions.
• Leads the use of the most efficient or innovative approach in evidence generation, ensuring the most appropriate designs for answering efficacy and safety questions to be submitted to external stakeholders. Demonstrates competency in justifying methodology selected.
• Leads statistical activities, with the development of protocols, analysis plans and execution, interpretation, and publication for non-interventional studies, Real World Evidence (RWE) research, data mining, and network meta-analyses/indirect comparisons.
• Leads statistical activities and work with cross therapeutic development team to develop statistical insights using real world data (Claim data, registry, EMR) to help with study design, portfolio strategy and study execution.
• Provide technical statistical leadership to data-related research in Health Technology Assessment (HTA) and reimbursement globally (US, Europe, Asia Pacific and other geographies) to help enhance the success of the compound considering agency requirements across the globe.
• Perform peer-review of work products from other statistical colleagues.
• Ensures high quality statistical support for projects through the oversight of CRO suppliers, and provide input into outsourcing strategy and processes

Training and Development

• Keep up to date with respect to statistical methodology, particularly in methods applicable to real-world data, real-world evidence, observational research, in Medical Affairs, and causal inference to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.

Communication of Results

• Collaborate with team members or external partners to communicate results.
• Assist with or be responsible for communicating study results via reimbursement dossiers/submissions, manuscripts, or oral presentations.
• Communicate results in one-on-one meetings with key customers or external partners and present at scientific and therapeutically focused meetings.

Therapeutic/Scientific Area Knowledge

• Understand disease states, competitive landscapes and reimbursement environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.

Regulatory Compliance

• Perform work in full compliance.