Research Scientist Computation
Company Name:
Eli Lilly
Responsibilities:
Statistical Analysis
Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.
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-reviewof work products from statistical colleagues.
Effectively utilize current technologies and available tools for conducting the clinical trial analysis.
Communication of Results and Inferences
Collaborate with other statistical colleagues to write reports and communicate results.
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.
Assist or respond to regulatory queries working in collaboration with other statistical colleagues.
Therapeutic Area and SystemsKnowledge
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.
The Project Statistician Computation at this level provides statistical leadership in multiple dimensions including:
Masters primary programming language and its capabilities in implementing any type of analysis or computation.
Applies innovative programming techniques to solve critical problems.
Collaborates with project statistician to suggest appropriate methodology.
Merges scientific thinking & business knowledge to identify & impact business issues.
Drives projects internally (or externally), and works effectively across functions.
Uses technical expertise to influence business decisions.
Identify broad technical issues, drives assessment of options and implements robust solutions
Basic Qualifications
Bachelor's degree in Statistics/ Biostatistics or related field with at least 15 years of clinical trial experience in pharmaceutical industry.
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
Additional Skills/Preferences
Proficiency in statistical programming languages/software such as SAS, R, Spotfire, WinBUG, etc.
Interpersonal/teamwork skills for effective interactions
Technical growth and application with working knowledge of statistics and statistical software
Self-management skills with a focus on results for timely and accurate completion of competing deliverables
Creativity and innovation
Demonstrated problem solving ability and attention to detail
Data analysis, technology, and systems expertise
Pharmaceutical industry standards such as ICH guidelines, SDTM, ADaM, CDISC, CDASH, etc., knowledge
Work and manage external vendors and third party organizations and provide oversight to outsourced work.
Apply online at: https://xjobs.brassring.com/tgwebhost/jobdetails.aspx?PartnerId=25428&SiteId=5645&Areq=11834BR&Codes=IMBEstimated Salary: $20 to $28 per hour based on qualifications.
Eli Lilly
Responsibilities:
Statistical Analysis
Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.
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-reviewof work products from statistical colleagues.
Effectively utilize current technologies and available tools for conducting the clinical trial analysis.
Communication of Results and Inferences
Collaborate with other statistical colleagues to write reports and communicate results.
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.
Assist or respond to regulatory queries working in collaboration with other statistical colleagues.
Therapeutic Area and SystemsKnowledge
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.
The Project Statistician Computation at this level provides statistical leadership in multiple dimensions including:
Masters primary programming language and its capabilities in implementing any type of analysis or computation.
Applies innovative programming techniques to solve critical problems.
Collaborates with project statistician to suggest appropriate methodology.
Merges scientific thinking & business knowledge to identify & impact business issues.
Drives projects internally (or externally), and works effectively across functions.
Uses technical expertise to influence business decisions.
Identify broad technical issues, drives assessment of options and implements robust solutions
Basic Qualifications
Bachelor's degree in Statistics/ Biostatistics or related field with at least 15 years of clinical trial experience in pharmaceutical industry.
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
Additional Skills/Preferences
Proficiency in statistical programming languages/software such as SAS, R, Spotfire, WinBUG, etc.
Interpersonal/teamwork skills for effective interactions
Technical growth and application with working knowledge of statistics and statistical software
Self-management skills with a focus on results for timely and accurate completion of competing deliverables
Creativity and innovation
Demonstrated problem solving ability and attention to detail
Data analysis, technology, and systems expertise
Pharmaceutical industry standards such as ICH guidelines, SDTM, ADaM, CDISC, CDASH, etc., knowledge
Work and manage external vendors and third party organizations and provide oversight to outsourced work.
Apply online at: https://xjobs.brassring.com/tgwebhost/jobdetails.aspx?PartnerId=25428&SiteId=5645&Areq=11834BR&Codes=IMBEstimated Salary: $20 to $28 per hour based on qualifications.
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