Lilly Assoc. Consultant, Computation in Shang Hai-上海, China
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 35,000 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.
Primary Function/Purpose：The Statistician-Computation assists during the development of data analysis plans in collaboration with statistical colleagues, physicians, and/or medical colleagues.The Statistician-Computation is responsible for establishing a reporting database and for analyzing clinical trial data by working with clinical research associates/clinical development associates and project statisticians. 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 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 data 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 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 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 technology advances.
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.
B.S, M.S, or equivalent experience
Statistics, Biostatistics, Computer Science, Epidemiology, or equivalent of field study
At least 2-5 years clinical trial working experience
Proficiency in the SAS programming language
R programming language is a plus
CDISC standard working experience is plus for P1 and required for P2
Interpersonal/teamwork skills for effectiveness 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 completing deliverables
Creativity and innovation
Demonstrated problem solving ability and attention to details
Data analysis, technology, and system expertise
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At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!