Statistical Programmer II
Parexel
full-time
Posted on:
Location Type: Remote
Location: United States
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About the role
- Work with Project Lead ADS to develop, validate, and maintain datasets and statistical outputs for clinical trials, including Study Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs), ensuring programming accuracy, traceability, and compliance with internal processes and regulatory expectations
- Develop and support programming outputs across a wide range of data types, including exploratory biomarker data and real-world data
- Collaborate on Exploratory Data Analyses (EDAs), enabling insight generation to inform drug development strategies and enhance scientific communication
Requirements
- Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field
- A minimum of 3 years of experience in statistical programming in a clinical development setting supporting Oncology trials/research, or an advanced degree with 1-3 years of equivalent work experience
- Proficient in and have recent working knowledge of SAS and R
- Basic understanding of statistical quality, endpoints, and QC processes
- Experience with Clinical Data Interchange Standards Consortium (CDISC) standards (e.g., SDTM and ADaM)
- Demonstrated ability to deliver programming outputs independently
- Fluent in English
Benefits
- EEO Disclaimer: Parexel is an equal opportunity employer.
- Qualified applicants will receive consideration for employment without regard to legally protected status.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
statistical programmingSASRdata validationdata maintenanceprogramming accuracytraceabilitycomplianceExploratory Data Analysesstatistical quality
Soft skills
collaborationindependent deliveryscientific communication