Rotation Descriptions

Global Operations Labeling Department

This rotation will provide the opportunity to work with various regulatory agencies in facilitating the creation and maintenance of global product information for commercialized products in development. This Department is responsible for the development and accurate updating of U.S. labeling documents, and providing therapeutic, process and regulatory expertise on labeling issues.

Cialis® Product Team

This rotation will see you gain an understanding of the clinical research process by focusing on the global development and marketing of our new PDE5 inhibitor. You will partner with colleagues on the clinical research global strategy, as well as the global marketing strategy.

Manufacturing

This rotation is ideal for individuals interested in industrial pharmacy and non-clinically oriented careers within the industry. Your strong interest in math, science and pharmaceutics will aid you with pilot and full-scale manufacturing of dry products with an emphasis on controlling quality. You will gain a hands-on knowledge of operations critical to tablet and capsule manufacturing, along with quality control.

Clinical Research

Gain first-hand knowledge of the clinical trial research required to evaluate the safety and efficacy of drugs in humans. You will witness the four phases of clinical trial research and learn about the regulatory requirements, good clinical practices, and corporate business goals that drive our work.

Global Scientific Information and Communications

The goal of this rotation is to provide insight into the communications and operational consulting services that optimize Lilly’s capability to gain rapid global regulatory approvals and effectively commercialize products. You will help provide clear, concise and accurate documentation of clinical information, and influence adherence to relevant policies and standards. Clinical Pharmacology Scientific Communications help clinical pharmacology team members plan, write and edit regulatory submissions related to clinical pharmacology studies.

Health Outcomes

This rotation will expose you to the decision-making process of allocating scarce health resources, and maximizing the understanding and utility of health outcomes information. By communicating innovative and credible health outcomes, you will help maximize patient outcomes and the value of our products.

Medical Information

This group supports the successful worldwide use of our products through preparing and disseminating global medical information in support of Lilly’s therapeutic areas. The U.S. Medical Information Services is in charge of providing real-time medical information, fulfillment of medical letters, reprints and literature searches for healthcare professionals and the launch of new products.

Medical Liaison

This rotation will see you develop and enhance Lilly’s relationship with leaders within the healthcare community. This team is in charge of contributing to improved health outcomes through the timely, responsive dissemination of medical information, exploring clinical, and scientific interests with health care providers, and supporting professional education.

Global Product Safety

The role of this group entails collecting information on adverse events, as well as monitoring, evaluating and communicating information to ensure the safe use of all our products. As part of this team, you will help with safety reports on Lilly compounds, adverse drug reports, regulatory inquiries, proactive safety surveillance, and maintaining and disseminating safety information.

Public Policy Planning and Development

In an effort to influence the external environment in which we operate, the members of this team identify, develop, communicate and assist groups in advocating our position on public policy issues. We develop public policies that are linked with our corporate priorities, and lead the development of compelling arguments and communications tools to positively influence these policy decisions.

U.S. Regulatory Affairs

This rotation will see you learn about the regulatory affairs process, including competitive intelligence and benchmarking projects. You will help support submissions of protocols, investigator documents, FDA responses, non-clinical documents, and investigational and pre-market approval registration dossiers.

Early Phase Clinical Research - Musculoskeletal

This area is critically important in assessing drug safety and efficacy, and determining the success of compounds for musculoskeletal activity. In this rotation, you will join an interdisciplinary team developing a clinical study strategy and plan, preparing study protocols and regulatory documents, and providing literature research and data analysis.