Principal Statistical Programmer: RWD/Epi (Remote)

Jobgether; United States; Remote; USD 150,000 - 210,000; Full time

Benefits offered by this job

Full-time remote work

Impactful RWE research

Multidisciplinary collaboration

Exposure to complex datasets

Job summary

Partner Company seeks a Principal Statistical Programmer FSP – RWD/EPI in the United States to advance real-world evidence research. You will transform healthcare data into insights, collaborating with epidemiologists, statisticians, and cross-functional teams to support observational studies and regulatory documentation.

You will program analyses, manage data, and contribute to Medical Affairs and Clinical Development activities while delivering timely analyses and reports for clients.

Qualifications

• Master’s degree or PhD in a quantitative field is required.
• At least 5 years of experience in real-world evidence analytics in pharma/CRO/academia.
• Proficiency in SQL is essential; SAS or R experience is required.

Responsibilities

• Prepare real-world data for epidemiology studies and advise on analysis strategies.
• Develop SAPs and study protocols for analyses using large real-world data sources (claims, EHR).
• Coordinate with data vendors to obtain data extracts per approved protocols.
• Build and maintain analytical databases to support statistical analyses.
• Program and conduct analyses, including coding, dataset linkage, and modeling.
• Generate tables, figures, and reports to communicate findings to investigators and clients.
• Support data visualization and reporting of observational data.

Skills

SQL

SAS/R

Real-world data

Education

Master’s or PhD in Epidemiology/Biostatistics/Statistics/Bioinformatics/related field

Tools

Optum Clinformatics Datamart®

Market Clarity

Truveta

UK Biobank

Job description

Partner Company seeks a Principal Statistical Programmer FSP – RWD/EPI in the United States to advance real-world evidence research. You will transform healthcare data into insights, collaborating with epidemiologists, statisticians, and cross-functional teams to support observational studies and regulatory documentation.

You will program analyses, manage data, and contribute to Medical Affairs and Clinical Development activities while delivering timely analyses and reports for clients.