Advisor

healthcare

Advisor-ComputationalStatistician

$152–244k Indianapolis, Indiana, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Advisor - Computational Statistician at Advisor. Skills: statistical analysis, statistical programming, SAS, R. Provide input to statistical analysis plans. Write reports and communicate results”

What You'll Achieve.

prompt and accurate completion of competing deliverables

Industry & Context.

healthcare
Problems you'll solve

Demonstrated problem solving ability; solve critical problems; Identify broad technical issues; Drives assessment of options; Implement robust solutions

What They're Looking For.

Must Have

Master’s degree in Statistics, Biostatistics, or MSPH with concentration in Statistics or Biostatistics, or relevant areas, 7+ years of statistical analysis/programming experience

Nice to Have

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

What You'll Do.

Provide input to statistical analysis plans

Write reports and communicate results

Assist/respond to regulatory queries

Select statistical methods for data analysis

Author sections of the analysis plan

Collaborate with data management in planning and implementation of data quality assurance plans

Maintain proficiency with respect to SAS programming and statistical methodology

Apply new and varied methods

Justify methods selected

Implement previously outlined analysis plans

Conduct peer-review of work products

Use current technologies and available tools for conducting clinical trial analysis

Assist in the communication of study results via regulatory submissions

Communicate one-on-one with key customers

Understand relevant disease states

Ensure replication of tools and systems

Stay informed of technological advances

Perform work in full compliance with assigned curriculum(s)

Follow applicable corporate

and departmental policies

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

Implement robust solutions

How You'll Work.

Team & Collaboration

Collaborate with other statistical colleagues and study personnel; Collaborate with data management; Collaborate with project statistician; Works effectively across functions

Communication Scope

communicate results; communication of study results; communicating one-on-one with key customers

Process & Methodology

Drives projects internally (or externally)

Full Job Description

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 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. **Responsibilities** **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 ass

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