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Eli Lilly and Company Research Scientist Statistics - R-7856 in Indianapolis, Indiana

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. Were 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 global 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.The Clinical Project Statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, clinical research scientists, and/or medical colleagues. The Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for clinical studies.Key Responsibilities:The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.Statistical Trial Design and AnalysisOperate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.Collaborate with data sciences in the planning and implementation of data quality assurance plans.Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.Maintain currency with respect to statistical methodologyInfluence team members regarding appropriate research methodsParticipate in peer-review of work products from other statistical colleagues.Perform peer-review of work products from other statistical colleagues.Communication of Results and InferencesCollaborate with team members to write reports and communicate results.Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.Respond to regulatory queries and interact with regulators.Support responses to regulatory queries and/or regulatory interactions.Therapeutic Area KnowledgeUnderstand disease states, competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.Regulatory CompliancePerform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.Statistical leadership and TeamworkIntroduce and apply innovative methodology and tools to solve critical problemsMerge scientific thinking and business knowledge to identify issues, evaluate options and implement solutions.Lead projects independently and work effectively across functions. Apply technical expertise to influence business decisions.Minimum Qualification Requirements:Ph.D. in Statistics OR BiostatisticsOther Information/Additional Preferences:Proficient in statistical programming languages/software such as SAS, R, Spotfire, WinBUG, etcInterpersonal communication skills for effective customer consultationTeamwo

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