Key Responsibilities:
- Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
- Support TLF generation, perform QC checks, and ensure regulatory compliance for clinical trial deliverables.
- Collaborate with biostatistics and clinical teams, and contribute to automation and documentation best practices.
Required Qualifications:
- Bachelor's or Master's degree in Statistics, Computer Science, or a related field with 4–6+ years in clinical programming.
- Proven experience creating SDTM and ADaM datasets using R and a solid understanding of CDISC standards.
- Working knowledge of SAS, experience with clinical trial data and regulatory submissions, and strong analytical skills.
Preferred Qualifications:
- Experience with R packages such as tidyverse or pharmaverse, and tools like R Markdown or Shiny apps.
- Exposure to GxP validation, version control with Git, and automated workflows in a CRO or pharmaceutical environment.
Company Culture:
- Operates as a global CRO with over 4,000 professionals, emphasizing diversity, inclusivity, and employee development as core assets.
- Maintains low industry-average turnover through continuous training and a mission to accelerate drug and device development.
ClinChoice
ClinChoice is a global contract research organization (CRO) that specializes in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals across more than 20 countries, it fosters a diverse and inclusive culture focused on employee development and low turnover through close management and continuous training.