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Statistical Programmer Analyst I/II -Permanent Role- Hybrid (2 days a week) at ClinChoice - ApplyBlast

Statistical Programmer Analyst I/II -Permanent Role- Hybrid (2 days a week)

ClinChoice

3 months ago

3.3 on Glassdoor

Remote

Full Time

Senior

0 applicants

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About this role

ClinChoice is seeking a Statistical Programmer Analyst to support clinical trial data analysis and reporting for a diverse portfolio of pharmaceutical and biotechnology clients. The role involves developing, validating, and maintaining statistical programs using SAS and R to generate Tables, Listings, and Figures (TLFs) while ensuring compliance with regulatory standards. Candidates will collaborate with biostatisticians and data management teams to deliver high-quality study outputs and support submission activities.

Responsibilities

Develop and validate statistical programs using SAS for clinical trial data
Perform data manipulation and analysis using R and SAS packages
Generate Tables, Listings, and Figures (TLFs) for study deliverables
Ensure compliance with regulatory standards and company SOPs
Conduct quality control and validation of programming outputs

Skills

Qualifications

Bachelor's degree in Statistics, Biostatistics, Computer Science, or related fieldMaster's degree in Statistics, Biostatistics, Computer Science, or related field

About ClinChoice

clinchoice.com

Headquarters

Horsham, Pennsylvania, United States

Company Size

1001-5000 employees

Founded

1995

View Profile

ClinChoice is a full‑service global contract research organization (CRO) that helps accelerate drug and medical device approvals to market. They offer end‑to‑end clinical development, regulatory strategy, and operational support across study design, execution, data management and safety to guide sponsors through all phases of development. With global site networks, therapeutic expertise and data‑driven processes, ClinChoice aims to shorten timelines and reduce risk for development programs. They partner with biotech, pharma and device companies to navigate complex regulatory pathways and bring safer products to patients.