Biostatistician II – Clinical Trials Analytics (Hybrid)

UW School of Medicine and Public Health

Madison (WI)

Hybrid

USD 73,000 - 90,000

Full time

6 days ago
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Benefits offered by this job

SMPH Faculty /Academic Staff Benefits

Job summary

The University of Wisconsin–Madison’s UW School of Medicine and Public Health is seeking a Biostatistician II to provide statistical insights for independent Data Monitoring Committees overseeing industry-sponsored clinical trials.

Responsibilities include designing methods, developing study designs, and contributing to manuscripts and reports while supporting data safety monitoring and regulatory requirements.

Qualifications

  • Experience in biostatistics, clinical trial design and implementation, data safety monitoring, industry clinical trials.
  • Excellent written and oral communication skills.
  • Experience working with data from large, multifaceted databases.

Responsibilities

  • Designs and implements statistical methods and applicable resource materials used for research projects
  • Develops research study designs for research projects
  • Contributes to preparing, writing, editing, and submitting research manuscripts, presentations, reports, research grant and contract proposals and/or post-award reports to funding agencies
  • Evaluates, prepares, analyzes, and interprets existing data and sources, selects and applies appropriate statistical methods, and prepares summarized reports
  • Advises on best practices and established policies, procedures, and regulations and conducts biostatistical analysis for internal and external stakeholder groups

Skills

SAS
S-PLUS
R
UNIX

Education

Master's Degree in Biostatistics

Tools

SAS
S-PLUS
R
UNIX

Job description

The University of Wisconsin–Madison’s UW School of Medicine and Public Health is seeking a Biostatistician II to provide statistical insights for independent Data Monitoring Committees overseeing industry-sponsored clinical trials.

Responsibilities include designing methods, developing study designs, and contributing to manuscripts and reports while supporting data safety monitoring and regulatory requirements.

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