Clinical R Programmer Consultant
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
Clinical R Programmer Consultant (R/Clinical Programming): Developing and validating SDTM and ADaM datasets and clinical trial reporting deliverables with an accent on CDISC compliance, reproducible R workflows, and regulatory-quality data products. Focus on building automated pipelines, reconciling clinical data issues, and supporting complex TLF generation across R and SAS.
Location: Remote within the United States.
Company
is a global full-service contract research organization providing clinical development and functional services to pharmaceutical, biotechnology, medical device, and consumer health companies.
What you will do
- Develop, validate, and maintain SDTM and ADaM datasets in R according to CDISC standards.
- Generate Tables, Listings, and Figures using R or SAS.
- Write reproducible R scripts for clinical data analysis and reporting.
- Collaborate with statisticians, data managers, and clinical teams to define programming requirements.
- Perform QC checks, reconcile data issues, and ensure regulatory-ready deliverables.
- Contribute to documentation, version control, automation, and R-based pipeline development.
Requirements
- Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field.
- 2–3+ years of clinical programming experience with a strong focus on R.
- Hands-on experience creating SDTM and ADaM datasets using R.
- Working knowledge of SAS programming and clinical trial data.
- Understanding of CDISC standards, regulatory submissions, and QC processes.
- Strong analytical, problem-solving, and documentation skills.
Nice to have
- Experience with tidyverse, haven, pharmaverse, admiral, tidyCDISC, or similar clinical programming toolkits.
- Knowledge of R Markdown, Shiny, or reproducible reporting tools.
- Exposure to GxP validation, Git, and automated workflows.
- Experience in a CRO or pharmaceutical environment.
Culture & Benefits
- Work directly with a single sponsor while receiving the career opportunities and support of a global CRO.
- Access to continuous training and professional development.
- Collaboration across teams in the Americas, Europe, and Asia-Pacific.
- Culture focused on quality, diversity, inclusion, and healthcare innovation.
Hiring process
- Submit a CV and receive confirmation of receipt.
- Qualified applicants are invited to a phone interview as the first step.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →