Senior Statistical Programmer Consultant at ClinChoice, Remote, £Contract Rate (Outside IR35)

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 Senior Statistical Programmer Consultant to join one of our clients in R&I team. 

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.  

Main Job Tasks and Responsibilities: 

The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks

Key Requirement:

• Strong SAS programming experience within the pharmaceutical/CRO industry
• Hands-on experience supporting Respiratory & Immunology (R&I) studies
• Experience in generating and validating SDTM, ADaM, and TLFs
• Good understanding of CDISC standards and clinical trial processes
• Ability to work independently and manage multiple priorities in a fast-paced environment
• Experience supporting regulatory submissions is preferred
• Strong communication and stakeholder management skills

Responsibilities:

• Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
• Create datasets, tables, listings, and figures according to study requirements
• Collaborate with Biostatistics, Data Management, and Clinical teams
• Ensure programming deliverables meet quality standards and project timelines
• Participate in study planning, review specifications, and support submission activities

Education and Experience:

• 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.
• Need to have Respiratory/Immunology TA experience.
• Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.