Senior/Principal R Programmer Consultant-Remote

ClinChoice

94d

About The Position

ClinChoice is searching for a Senior/Principal R Programmer Consultant to join one of our clients. The Senior Clinical Programmer with advanced expertise in SAS, R, and Power BI to support clinical trial data analysis, reporting, and visualization. In this role, you will lead programming activities across multiple studies, ensuring high-quality and regulatory-compliant deliverables while enabling data-driven insights through interactive visualizations. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

Requirements

• Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or related field.
• 5+ years of experience in clinical programming within pharmaceutical, biotech, or CRO environments.
• Expert-level programming skills in SAS (Base, Macro, SQL) and strong experience with R (including packages like tidyverse, haven, ggplot2).
• Proficiency in developing dashboards and reports using Power BI (including DAX and Power Query).
• Solid knowledge of CDISC SDTM and ADaM standards and experience applying them in clinical trials.
• Familiarity with regulatory submission requirements and documentation for FDA/EMA.
• Strong analytical, problem-solving, and organizational skills.
• Ability to manage multiple priorities and work collaboratively across cross-functional teams.

Responsibilities

• Develop, validate, and maintain analysis datasets (SDTM/ADaM), Tables, Listings, and Figures (TLFs) in support of clinical trial reporting using SAS and R.
• Design and implement data visualization dashboards in Power BI to support clinical development teams, safety monitoring, and cross-functional data reviews.
• Collaborate closely with biostatistics, data management, clinical operations, and other functional teams to ensure accurate, timely, and efficient programming deliverables.
• Contribute to the development, refinement, and documentation of standard macros, templates, and programming processes.
• Participate in the review of study protocols, CRFs, and statistical analysis plans (SAPs) to ensure alignment with data reporting and visualization strategies.
• Ensure compliance with CDISC standards (SDTM, ADaM) and applicable regulatory requirements (e.g., FDA, EMA).
• Provide technical mentorship and support to junior programmers and contribute to training initiatives.
• Lead or contribute to programming activities in support of regulatory submissions (e.g., define.xml, reviewer guides, data packages).

What This Job Offers

• Career Level: Senior
• Education Level: Bachelor's degree
• Number of Employees: 51-100 employees