Senior Clinical Programmer

Senior Clinical Programmer at Cytel in Boise, Idaho, United States Job Description We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position requires a solid understanding of clinical trials, data integration, and programming techniques to support the creation, validation, and execution of clinical study data in a fast-paced environment.

Key Responsibilities:

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Programming and Development:

Write and maintain code for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment. +

Data Management and Quality:

Ensure accurate and timely delivery of clinical trial data by performing data checks, validation, testing, and reconciliation in line with clinical trial timelines and regulatory requirements. +

Collaboration:

Work closely with clinical data managers, statisticians, and other stakeholders to design and implement clinical data flow, ensuring compliance with all regulatory requirements. +

Troubleshooting and Issue Resolution:

Identify, investigate, and resolve any issues that arise within the platform or clinical data programming processes. +

Documentation:

Maintain comprehensive documentation of programming processes, code, and data management workflows for audit and regulatory purposes. +

Continuous Improvement:

Contribute to the improvement of programming practices, tools, and templates to streamline clinical programming workflows and enhance efficiency. +

Training and Mentorship:

Provide guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating knowledge sharing within the team. +

Experience:

4-6 years of experience in clinical programming. +

Technical Skills:

+ Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.). + Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and programming solutions. + Strong knowledge of clinical trial data structures, data standards (e.g., CDISC, SDTM), and regulatory requirements (e.g., FDA, EMEA). +

Problem-Solving:

Excellent troubleshooting and problem-solving skills with the ability to work under pressure to meet deadlines. +

Communication:

Strong communication skills with the ability to collaborate effectively with

Job Posting:

JC290961920

Posted On:

Apr 24, 2026

Updated On:

Apr 24, 2026