Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior R Developer

6+ years
Not Disclosed
10 Feb. 10, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior R Developer

Excelya | Full-time | Permanent Contract | Remote (Europe)

Excelya, a leading Contract Research Organization (CRO) in Europe, is seeking a Senior R Developer to develop R packages supporting metadata-driven SDTM automation in clinical research. This role involves end-to-end development, package management, and regulatory reporting while collaborating with a team of software engineers.

Key Responsibilities

R Development & Clinical Data Automation

  • Design and develop R packages to streamline SDTM automation.
  • Implement CDISC SDTM & ADaM datasets using R.
  • Lead the development and technical implementation of all R packages in the project.
  • Write comprehensive documentation, unit tests, and integration tests for R packages.

Code Management & Collaboration

  • Manage package versioning in GitLab.
  • Perform hands-on programming and code reviews.
  • Support open-sourcing initiatives for R packages.

Clinical Data Standards & Regulatory Compliance

  • Implement CDISC standards (SDTM/ADaM) in clinical research data.
  • Work on regulatory reporting for clinical trials using R or SAS.
  • Experience in SDTM pooling and submission processes (e.g., define.xml).

Minimum Requirements

  • 6+ years of professional experience in R development.
  • Strong experience in CDISC SDTM/ADaM implementation.
  • Experience in early or late-phase clinical trials and regulatory reporting.
  • Advanced proficiency in R, R package development, R Markdown, and R Studio.
  • Understanding of open-source software development principles.
  • Critical thinking and ability to lead multiple R package developments.
  • Excellent communication skills (working with experts & non-experts).

📍 Location: Remote (Europe)
Start Date: ASAP