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.

The primary responsibility of the US Medical Affairs CRP is to provide expert medical and scientific support to all aspects of the business, to ultimately improve outcomes for those with cancer. This includes support for drugs in development, marketed products, and the disease state.

The CRP plays a leadership role in understanding the therapeutic environment and HCP needs, generating critical scientific evidence, and disseminating scientific data. The core job responsibilities may include those listed below as well as other duties as assigned.

Environmental Insights and Customer Engagement

Understand and anticipate the scientific information needs of customers (oncologists, payers, patients, health care providers)Engage external customers through 1:1s, advisory boards, and congress-related activitiesBuild and cultivate key oncology thought leader relationshipsContribute to the development of medical strategies to support pre- and post-commercialization activities by working closely with the Global Medical Affairs, clinical development and brand teamsIdentify and deliver solutions to close oncology/hematology clinical care gapsSupport internal field training of medical and commercial personnelDevelop and maintain appropriate collaborations and relationships with relevant professional societiesStay on the cutting edge of emerging data/science sharing key trends and data that could inform strategyDevelop and deliver scientific and medical presentations, organize and lead medical advisory boards, participate in investigator meetings, provide medical support to commercial advisory boards.  Identify relevant medical meetings and congresses; determine appropriate participation (Med Affairs station, abstracts, posters, etc.).Assist in the selection of outside experts and clinical advisors as well as maintain key relationships of mutual interest around clinical trials, guidelines and advisory boards. Ensures Medical Affairs participation in Legal, Medical, Regulatory Review Committee. Reviews advertising and promotional, as well as scientific and educational materials.

Evidence Generation

Identify evidence gaps and develop evidence generation proposals to address suchActively address customer questions in a timely fashion by leading data analyses and new clinical or health outcomes research effortsCollaborate with clinical development to inform drug development plans and clinical trialsParticipate in investigator identification and selection, in conjunction with clinical development teamsInform collaborative and investigator-initiated research (IIR) plan and publications, as requested

Scientific Data Dissemination/Exchange

Understand and actively address the scientific information needs of external customers in accordance with global proceduresAnalyze, interpret, and translate scientific data in order to generate scientific disclosuresSupport medical education initiatives including congress symposia, CME, and omnichannel educationReview and inform medical letters, slide decks, and other medical information materialsOffer scientific and creative input to contribute to the development, review, and approval of promotional materials for the commercial brand teamGenerate and deliver medical and disease state educational solutions including input into Global clinical care gaps

General Responsibilities

Effectively partner internally and externally to execute medical prioritiesWork seamlessly across the enterprise to effectively lead cross-functional initiativesAdapt quickly with the ever-changing clinical landscape and/or program prioritiesEffectively communicate up, down, and across the organizationShape hematology strategy and execution plans including training and onboarding of medical team members.

Basic Requirements:

Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiringMust have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see http://www.in.gov/pla/2799.htm2-5 years in medical affairs or clinical development or equivalent. 

Additional preferences:

Experience in Oncology/Hematology, with specific direct knowledge and experience in B-cell leukemias and lymphomas malignancies such as CLL and mantle cell lymphoma preferableExperience launching Oncology product is desired; Prior launch experience in CLL space highly desirable.Demonstrated ability to balance scientific priorities with business prioritiesDemonstrated strong communication, interpersonal, teamwork, organizational and negotiation skillsDemonstrated ability to influence others (both cross-functionally and within your function)Ability to engage in domestic and international travel to the degree necessary to support the businessFluent in English, verbal and written communicationUnderstanding of the US healthcare system, regulatory and relevant payer environment

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 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.

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