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1023# Principal R Programmer – Hematology Permanent remote role at ClinChoice. . Location: United States.  . . 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.. . #LI-TT1 #LI-Remote #LI-Principal . .  . .