Job Details
Principal Statistical Programmer
5542
Posted: 29/04/2025
- £Competitive
- Home Based , , United Kingdom
- Permanent
Principal Statistical Programmer | Leading CRO | Home Based | UK |
Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries
Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career.
To drive continued success in this exciting clinical research field, there is an opportunity to join this team as Principal Statistical Programmers remotely in the UK.
What you will be doing:
What you will need:
What in it for you:
What to do next:
Not what you’re looking for?
Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries
Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career.
To drive continued success in this exciting clinical research field, there is an opportunity to join this team as Principal Statistical Programmers remotely in the UK.
What you will be doing:
- Lead complex statistical programming projects, ensuring timely, high-quality deliverables and client satisfaction.
- Serve as a client liaison for programming-related discussions, proposals, and bid defence
- Mentor junior programmers and provide technical training and oversight.
- Develop, program, and validate SDTM and ADaM datasets for CSRs, ISS, and ISE, following CDISC standards.
- Conduct quality reviews and resolve Pinnacle 21 validation issues.
- Generate and QC define.xml files and documentation for regulatory submissions.
- Lead or support submission-related programming activities, including QC of datasets and outputs.
- Create, validate, and maintain macros and tools to support programming efficiency.
- Ensure compliance with company and sponsor SOPs, training, and documentation standards.
- Oversee data archiving and support client cluster programming as needed.
What you will need:
- A Master’s or Ph.D. degree in Statistics, Biostatistics or Epidemiology.
- At least 10 years’ experience in clinical trial Statistical Programming.
- Excellent knowledge of SAS essential with R advantageous.
- Good working knowledge of data structures e.g. CDISC, SDTM, ADaM,
- Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines.
What in it for you:
- The opportunity to be involved in a growing organisation.
- Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
- Fully remote in the UK
- Generous remuneration package.
What to do next:
- If this opportunity is of interest, please apply now with your CV as the organisation are looking to arrange interviews for the Principal Statistical Programmer as soon as possible.
Not what you’re looking for?
- Please contact Jo Fornaciari on +44 7488 822 859 for a confidential discussion about potential opportunities.
Jo Fornaciari
Principal Consultant in Statistical Programming
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