Senior Statistical Programmer
Remote (US-based)
Full-time Permanent
We're partnering with a well-established, global clinical research organisation that provides full-service support to the pharmaceutical, biotechnology, and medical device industries. With a strong reputation for quality, flexibility, and customer focus, they are continuing to expand and are now seeking a Senior Statistical Programmer to join their growing team.
This is an opportunity to contribute to high-impact clinical trials within a collaborative, technically driven environment, working on innovative therapies and advancing global healthcare.
The Role
As a Senior Statistical Programmer, you will be responsible for the design, development, and validation of clinical trial datasets and outputs, ensuring compliance with industry standards and sponsor requirements.
You will play a key role in delivering high-quality programming outputs across studies, while also supporting and mentoring junior team members and contributing to process improvement initiatives.
Key Responsibilities
- Design and specify study data tabulation models and analysis data models (e.g. SDTM, ADaM)
- Develop and validate datasets in line with industry standards and study requirements
- Program and generate statistical outputs and reports using SAS
- Independently validate outputs and datasets created by other programmers/statisticians
- Develop and test SAS code for data checks and ongoing data review
- Ensure all programming documentation is accurate and compliant with SOPs
- Support data archiving activities in line with regulatory requirements
- Provide technical guidance and mentorship to junior programmers
- Contribute to the development of programming standards and best practices
- Support continuous improvement initiatives within statistical programming
Requirements
- Master's degree in Mathematics, Statistics, or a related field
- Minimum 5+ years' experience in statistical programming within clinical trials
- Strong expertise in SAS programming
- Experience working with clinical trial datasets and regulatory standards
- Strong understanding of data structures and statistical reporting
- Ability to work independently and collaboratively in a global team
- Excellent attention to detail and problem-solving skills
- Experience mentoring or supporting junior colleagues is advantageous
What's on Offer
- Fully remote working within the US
- Opportunity to work with a leading global CRO
- Exposure to a wide range of therapeutic areas and global studies
- Supportive, collaborative, and growth-oriented environment
- Strong focus on quality, innovation, and professional development
If you're an experienced Statistical Programmer looking to take the next step in your career within a high-quality, globally recognised CRO, we'd love to hear from you.
Apply now or get in touch for a confidential conversation.