1023# Principal R Programmer – Hematology Permanent remote role
Are you interested in working directly with a single sponsor while enjoying the security and global opportunities that come with being part of a leading CRO? Our team believes it’s the best of both worlds.
ClinChoice is seeking a Principal R Programmer in a FTE set up to join one of our key clients in their Hematology team. This client-dedicated role is ideal for confident professionals who thrive in a collaborative environment and are comfortable working independently while building strong, trust-based relationships with sponsor counterparts.
About ClinChoice:
ClinChoice is a global full-service CRO focused on quality, professional development, and a supportive, inclusive culture. We offer unique client-dedicated roles that allow you to build deep domain knowledge while benefiting from our international resources and career pathways.
Main Job Tasks and Responsibilities:
As a Principal R Programmer Consultant, you will lead and support all statistical programming activities aligned with project strategies. You’ll use R to create high-quality clinical deliverables and validate outputs using SAS, ensuring integrity and compliance across all submissions. This role demands high technical skill, strong clinical domain knowledge, and the ability to operate independently.
Key Responsibilities:
• Develop Tables, Listings, and Figures (TLFs) using R, referencing existing templates when available, or programming from scratch when needed.
• Author and maintain reusable R macros/functions to support consistent and efficient programming.
• Validate R-based outputs and deliverables against SAS results or legacy code to ensure consistency and compliance.
• Customize outputs and visualizations based on statistical analysis plans and targeted audience requirements.
• Take ownership of programming deliverables for clinical studies or projects, maintaining high quality and efficiency.
• Actively contribute to process improvement, programming standards, and best practices within the team.
• Ensure compliance with CDISC standards and maximize automation and reusable code.
• Coordinate programming activities, anticipate resource needs, and support timelines.
• Proactively identify and communicate risks or issues related to assigned studies/projects.
Education and Experience:
• Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field with 8+ years of clinical programming experience (CDISC); Master’s degree with 7+ years.
• Strong experience with R, including writing custom macros/functions and automating workflows.
• Ability to validate deliverables using SAS, with working knowledge of SAS as needed for verification tasks.
• Proven experience in the Hematology/Oncology therapeutic area is required.
• Hands-on experience with ISS and ISE deliverables.
• Solid understanding of ICH-GCP, clinical trial processes, and regulatory requirements.
• Strong communication, collaboration, and organizational skills.
• Up-to-date knowledge of clinical data standards and submission requirements (e.g., CDISC SDTM, ADaM).
Why ClinChoice?
• Work with a world-class team of experts on impactful clinical research.
• Grow your career with training, mentorship, and global project exposure.
• Enjoy a supportive, flexible, and collaborative work environment.
Ready to join a company that values both your technical expertise and your professional growth? Apply today and make an impact with ClinChoice.
Apply Now
ClinChoice is seeking a Principal R Programmer in a FTE set up to join one of our key clients in their Hematology team. This client-dedicated role is ideal for confident professionals who thrive in a collaborative environment and are comfortable working independently while building strong, trust-based relationships with sponsor counterparts.
About ClinChoice:
ClinChoice is a global full-service CRO focused on quality, professional development, and a supportive, inclusive culture. We offer unique client-dedicated roles that allow you to build deep domain knowledge while benefiting from our international resources and career pathways.
Main Job Tasks and Responsibilities:
As a Principal R Programmer Consultant, you will lead and support all statistical programming activities aligned with project strategies. You’ll use R to create high-quality clinical deliverables and validate outputs using SAS, ensuring integrity and compliance across all submissions. This role demands high technical skill, strong clinical domain knowledge, and the ability to operate independently.
Key Responsibilities:
• Develop Tables, Listings, and Figures (TLFs) using R, referencing existing templates when available, or programming from scratch when needed.
• Author and maintain reusable R macros/functions to support consistent and efficient programming.
• Validate R-based outputs and deliverables against SAS results or legacy code to ensure consistency and compliance.
• Customize outputs and visualizations based on statistical analysis plans and targeted audience requirements.
• Take ownership of programming deliverables for clinical studies or projects, maintaining high quality and efficiency.
• Actively contribute to process improvement, programming standards, and best practices within the team.
• Ensure compliance with CDISC standards and maximize automation and reusable code.
• Coordinate programming activities, anticipate resource needs, and support timelines.
• Proactively identify and communicate risks or issues related to assigned studies/projects.
Education and Experience:
• Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field with 8+ years of clinical programming experience (CDISC); Master’s degree with 7+ years.
• Strong experience with R, including writing custom macros/functions and automating workflows.
• Ability to validate deliverables using SAS, with working knowledge of SAS as needed for verification tasks.
• Proven experience in the Hematology/Oncology therapeutic area is required.
• Hands-on experience with ISS and ISE deliverables.
• Solid understanding of ICH-GCP, clinical trial processes, and regulatory requirements.
• Strong communication, collaboration, and organizational skills.
• Up-to-date knowledge of clinical data standards and submission requirements (e.g., CDISC SDTM, ADaM).
Why ClinChoice?
• Work with a world-class team of experts on impactful clinical research.
• Grow your career with training, mentorship, and global project exposure.
• Enjoy a supportive, flexible, and collaborative work environment.
Ready to join a company that values both your technical expertise and your professional growth? Apply today and make an impact with ClinChoice.
Apply Now