Principal Statistical Programmer /Analyst Consultant -CVRM at ClinChoice in United Kingdom
- Company: ClinChoice
- Location: United Kingdom
- Posted: Sep 20, 2026
- Type: Full-time
- Experience: 6+ years
Overview
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our…
Job description
- Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
- ClinChoice is searching for a Principal Statistical Programmer Consultant to join one of our clients.
- ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Responsibilities
- Leading statistical programming activities for clinical trials
- Developing/reviewing SAS programs, datasets, tables, listings, and figures
- Providing technical guidance to Statistical Programmers
- Reviewing programming specifications and outputs
- Supporting SDTM/ADaM and regulatory submissions
- Working closely with statisticians, data managers, and clinical teams
- Taking ownership of programming deliverables and timelines
- Mentoring junior and senior programmers
Requirements
- Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience.
- Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
- Good understanding of the clinical drug development process.
- Strong communication skills and coordination skills.
- Current knowledge of technical and regulatory requirements relevant for the role
- Ability to proactively manage concurrent activities within a project
- Proficient ability to influence relevant stakeholders on programming-related items
Skills
Required
- SAS programming
- CDISC standards
- ICH and Good Clinical Practices
- Regulatory requirements and terminology
- Clinical drug development process
- Communication skills
- Coordination skills
- Technical and regulatory requirements
- Influence stakeholders
About ClinChoice
About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.