This job is currently Archived,
Posted on : 23 May 2017
Req ID 33593 Title Clinical Research Physician-FDE City Indianapolis State / Province Indiana Country United States Company Overview 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 39,000 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. Responsibilities Serve as Clinical Research Physician with dual opportunities to support the development of early portfolio programs. ) )The Clinical Research Physician (CRP) is a leader in the oncology drug development team who guides creation of development strategy as well as the conduct and reporting of global clinical trials to support regulatory interactions, registration, and delivery of innovative treatments that improve the outcomes of people living with cancer. A CRP is a technical leader capable of sharing knowledge of cancer biology, pharmacology, clinical care expertise, translational research, and trial expertise. CRPs collaborate across geographies and functional areas of drug development to integrate knowledge, coordinate efforts, innovate to overcome challenges, and deliver rigorous data packages to support objective critical evaluation of experimental therapeutics. CRPs work closely with and inspire preclinical drug discovery teams to shape the next generation of novel therapeutics through experimental design and interpretation. CRPs play a key role in the publications and data dissemination for products and trials, and they must demonstrate confidence in discussion and presentation of technical content. 33593BR Basic Qualifications MD plus completion of Fellowship programPhysicians trained outside the US who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer. Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME) Additional Skills/Preferences Must be able to demonstrate basic knowledge of the drug development process and exercise Good Clinical Practice (ICH GCP) principles.Must be fluent in English; both written and verbal communications.Able to demonstrate strong communication, interpersonal, organizational, and negotiating skills.Must be able to demonstrate the ability to influence others (both cross-functionally and within the function) in order to create a positive working environment.Able to engage in domestic and international travel to the degree appropriate to support project and business needs.Previous research experience basic and/or translation is desirable.Demonstrated experience and involvement in clinical trial design or execution.Regulatory experience in support of INDs, BLAs, NDAs, supplemental applications etc. is desirable. Additional Information This position is not permanent. It is for a fixed duration of two years with potential to extend annually for up to 4 years.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.
Indiana, United States
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