Senior Statistical Programmer/Analyst Consultant- (Respiratory & Immunology) (Outside IR35) Uni[…]

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Senior Statistical Programmer/Analyst Consultant- (Respiratory & Immunology) (Outside IR35)

United Kingdom

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 Requirements

  • 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 years of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 years 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.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

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Company: ClinChoice Inc.
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Senior Statistical Programmer/Analyst Consultant- (Respiratory & Immunology) (Outside IR35)

United Kingdom

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 Requirements

  • 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 years of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 years 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.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

#J-18808-Ljbffr…

Posted: May 17th, 2026