Research Scientist- Clinical Project Statistician

Job Listing No: 9740000

Research Scientist- Clinical Project Statistician

??Company OverviewElanco is a global research-based company that develops and delivers product and services to enhance animal health and production. We value innovation, both in scientific research and daily operations, and strive to cultivate a collaborative work environment for more than 7,000 employees worldwide. Founded in 1954, Elanco is a division of Lilly. Our worldwide headquarters and research facilities are in Greenfield, Indiana.ResponsibilitiesJob Summary:Provide statistical expertise for the design and execution of clinical and drug product experiments during the development of food animal pharmaceuticals. ?Including statistical approaches, study design and data analysis to ensure scientifically robust and valid approaches. ?Serve as a key contributor of expertise in statistics to global product development teams.Role and Responsibilities:Make recommendations to product development & research teams, management and corporate strategy related to rationale and scientifically accurate strategies regarding the statistical analysis and scientific design of clinical and drug product experiments in support of development and registration of novel pharmaceutical products for food producing animalsMaintain current knowledge of publications and scientific progress in areas of applied statistics and biostatisticsAct and be recognized as an internal and external thought leader in statisticsFacilitate efficient knowledge sharing across Elanco to ensure robust problem solvingPromote collaborative environment and entrepreneurial mindset through modeling of the Elanco valuesProactively and collaboratively provide recommendations and guidance to product development teams and management for creative and strategic options for the statistical evaluation of product efficacy, safety and qualityIdentify and partner with external research or development organizations as appropriateAssist in drafting regulatory submissions and participate during dossier review processDirect involvement in discussions with global regulatory authorities in planning and implementation of development programs and support of active registrationsMonitor and ensure appropriate quality standards are maintained at all timesProvide data in a timely fashion to ensure accurate tracking of project budgets and timelinesEnsure scientific integrity and animal welfare in all activitiesBasic Qualifications?? ?PhD in biostatistics or statistics?Clinical study design experience through 3 months internship in industry or academia.Additional Skills/Preferences?? ?Familiar with GCP / GLP process, documentation and execution highly desired. ?Excellent written and verbal communication skills.Animal Health or Pharmaceutical experience preferredAdditional InformationLilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexualorientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.Removal Date:?? ?24-May-2017

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