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# RWE Biostatistician, Statistical Analyst/Programmer (Remote)

- **Company:** Techdata Service Company LLC
- **Location:** United States (Remote available)
- **Experience:** Experienced
- **Salary:** $100,000.0 - $210,000.0
- **Contract:** Permanent contract
- **Skills:** Data Analysis, Databases, R (Programming Language), SAP (Applications), SAS (Software), Data Management
- **Published:** May 17, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=3d69795ba005c8d5

## About the Role

Do you have experience in Statistics?, * Working knowledge and experience with bio statistical analysis and R and/or SAS programming.

 * Excellent oral and written communication skills in English are a must.
 * Prior work experience in epidemiology, health economic and outcome research, or clinical research area is a plus.
 * Specific experience and understanding of outcomes research, drug development is an asset
 * Familiarity with observational databases desirable; database examples
 * US medical and pharmacy claims databases (e.g. MarketScan)
 * US medical record databases (e.g. GE Healthcare)
 * US government public use databases (e.g. NHANES, MEPS)
 * Ph.D. in Statistics, epidemiology or related field, or MS with Minimum 2-year experience in pharmaceutical industry; Strong R programming skills.

## Description

TechData is looking for Real World Evidence (RWE) Biostatisticians or Statistical Analyst for our pharmaceutical clients. Please see below requirements.

Roles/Responsibilities

 * Utilize statistical knowledge of and expertise to provide statistical support for RWE studies, with a main focus of real-world observational studies, database examples:
 * Observational clinical studies, US medical and pharmacy claims databases (e.g. MarketScan, Optum); 2) US medical record databases (e.g. GE Healthcare);
 * Specify the structure of the datasets that will be delivered for statistical analysis to ensure that the structure follows any existing company standard for databases pooling.
 * Mock-up, review, and approve tables, listings and graphs specifications.
 * Establish/negotiate timelines for completion of study-related statistical activities. Ensure the study timelines are met.
 * Conduct observational data analysis, include data management, statistical programming, interpretation of analyses results, and write-up/review the corresponding sections of RWE study report.
 * Produce analysis datasets, listings, tables, and figures for research projects, according to specifications, while maintaining documentation and complying with pre-defined project / study standards.
 * Provide oversight of the biostatistics-related activities for RWE studies subcontracted to a CRO:
 * Perform quality control procedures to ensure that statistical deliverables conform to the requirements outlined in the SAP


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