About The Position

ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. This is a client-facing role where candidates are expected to work independently while establishing a high-trust environment with the client’s counterparts. 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.

Requirements

  • Strong SAS programming experience within the pharmaceutical/CRO industry
  • Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) 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
  • Strong communication and stakeholder management skills
  • 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.

Nice To Haves

  • Experience supporting regulatory submissions is preferred

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
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