848#Senior/Principal Statistical Programmer Consultant with R/R Shiny (Remote)

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...

ClinChoice is searching for a  Senior/Principal Statistical Programmer Consultant with R/R Shiny  to join one of our clients. 

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.

We are seeking a Senior Statistical Programmer with strong experience in R, R Shiny , and SAS to support clinical trial analysis and reporting for a leading pharmaceutical client. The ideal candidate will work closely with biostatisticians, data managers, and other programmers to deliver high-quality statistical outputs in compliance with regulatory standards.

Key Responsibilities:

• Develop, validate, and maintain statistical programs using R, R Shiny , and SAS to support clinical study reports (CSRs), regulatory submissions, and ad hoc analyses.


• Create interactive data visualizations and dashboards using R Shiny .


• Collaborate with biostatistics and data management teams to ensure accurate analysis and reporting of clinical data.


• Generate tables, listings, and figures (TLFs) per specifications.


• Ensure adherence to CDISC (SDTM/ADaM) standards and FDA/EMA regulatory guidelines.


• Participate in code reviews and ensure high-quality programming practices.


• Document programming processes and outputs thoroughly for audit readiness.

Required Qualifications:

• Bachelor’s or Master’s degree in Statistics, Computer Science, or a related field.


• 5+ years of experience in statistical programming in the pharmaceutical or CRO industry .


• Proficiency in R and R Shiny for statistical analysis and visualization.


• Strong experience with SAS for clinical trial programming.


• Knowledge of CDISC standards (SDTM and ADaM).


• Excellent problem-solving and communication skills.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.