Statistical Analysis:Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results, assist/respond to regulatory queries. Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created. Collaborate with data management in the planning and implementation of data quality assurance plans. Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods. Effectively justify methods selected and implement previously outlined analysis plans. Conduct peer-review of work products from statistical colleagues. Effectively use current technologies and available tools for conducting the clinical trial analysis. Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers. Therapeutic Area and Systems Knowledge:Understand relevant disease states in order to enhance the level of customer focus and collaboration. Ensure replication of tools and systems, where applicable and stay informed of technological advances. Regulatory and Quality Compliance:Perform 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. This role provides statistical leadership in multiple dimensions including:Masters primary programming language and its capabilities in implementing any type of analysis or computation. Apply innovative programming techniques to solve critical problems. Collaborate with project statistician to suggest appropriate methodology. - Merges scientific thinking & business knowledge to identify & impact business issues. Drives projects internally (or externally), works effectively across functions. Use technical expertise to influence business decisions. Identify broad technical issues, drives assessment of options and implement robust solutions. Basic Qualifications Master’s degree in Statistics, Biostatistics, or MSPH with concentration in Statistics or Biostatistics, or relevant areas . years of statistical analysis/programming experience. Additional Skills/ Preferences. Proficiency in statistical programming languages/software such as SAS, R, Spotfire, etc. Interpersonal/teamwork skills for effective interactions. Technical growth and application with solid understanding of statistics and statistical software. Self-management skills with a focus on results for prompt and accurate completion of competing deliverables. Creativity and innovation. Demonstrated problem solving ability and attention to detail. Data analysis, technology, and systems expertise. 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 ( 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 proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.