Scientist III

University of Wisconsin-Madison

. Lead study teams providing independent statistical data analysis to Independent Data Monitoring Committees monitoring the safety of industry-sponsored clinical trials .

Posted 10/9/2026full-timeMadison • Wisconsin • United StatesMid-LevelSenior💰 $90,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical data analysis and clinical trial design, with a strong focus on supervising research teams and liaising with stakeholders. Proficient in developing research methodologies and managing program budgets while ensuring effective communication and presentation of results.

Highest-signal resume keywords

Statistical Data AnalysisClinical Trial DesignPhD In BiostatisticsSAS And R ExperienceResearch Methodology Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical Data AnalysisClinical Trial DesignResearch Methodology DevelopmentData Science TechniquesComplex Data Analysis

Soft Skills

Excellent Written CommunicationExcellent Oral CommunicationSupervisory Skills

Tools & Technologies

SASRLinuxUNIX

Certifications & Qualifications

PhD In Biostatistics

Industry Keywords

Clinical TrialsIndependent Data Monitoring CommitteesResearch ProposalsGrant ApplicationsProgram Budgets

Tech Stack

Tools & technologies

LinuxUnix

About the role

Key responsibilities & impact

Lead study teams providing independent statistical data analysis to Independent Data Monitoring Committees monitoring the safety of industry-sponsored clinical trials
Prepare data sets, analyze them using data science techniques, and present results
Directly supervise study staff
Serve as an institutional subject matter expert and liaison with internal and external stakeholders
Identify research problems and develop complex research methodologies and procedures
Publish and present results
Supervise day-to-day activities of a research unit and staff and resolve routine personnel issues
Identify, write, or assist in developing grant opportunities, applications, and proposals
Facilitate scholarly events and presentations
Conduct literature reviews and prepare reports and materials
Monitor program budgets and approve unit expenditures
Collect and analyze complex research data, conduct experiments and interviews, and document results

Requirements

What you’ll need

Experience with analysis of clinical trial data
Experience with design of clinical trials
Excellent written and oral communication
PhD in biostatistics, or closely related quantitative discipline, is required
University sponsorship is not available, including transfers of sponsorship and TN visas
Must maintain continuous eligibility to work in the United States without employer sponsorship
Must provide proof of work authorization and eligibility to work
Cover letter required
Resume required
References will be requested from final candidates
Preferred: Experience with SAS and R in a Linux or UNIX environment

Benefits

Comp & perks

generous vacation, holidays, and sick leave
competitive insurances and savings accounts
retirement benefits