Senior Statistical Programmer​/Analyst Consultant; solid oncology background) Remote

United States

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….

Clin Choice is searching for a Senior Statistical Programmer Consultant
to join one of our clients.

Clin Choice 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.

We are seeking an experienced Senior Statistical Programmer with strong expertise in clinical trial programming and a solid background in oncology
. The successful candidate will be capable of independently leading statistical programming activities across clinical studies, partnering closely with statisticians, clinical teams, and other cross-functional stakeholders.

This role requires strong technical expertise in SAS programming, CDISC standards, and clinical trial reporting
, along with the ability to take ownership of programming deliverables and provide guidance to junior team members.

• Lead statistical programming activities for clinical studies within the oncology therapeutic area
  , from study start-up through database lock, analysis, and reporting.
• Develop, review, and maintain high-quality SAS programs for SDTM, ADaM, Tables, Listings, and Figures (TLFs).
• Lead programming activities for interim and final analyses, including complex efficacy and safety analyses.
• Work closely with Biostatisticians to understand statistical analysis plans, programming specifications, and study requirements.
• Develop and review programming specifications and ensure consistency with study protocols, SAPs, and statistical methodology.
• Support the creation and validation of CDISC-compliant SDTM and ADaM datasets
  .
• Generate and validate TLFs for clinical study reports, regulatory submissions, and other clinical deliverables.
• Perform independent programming validation and quality control of statistical outputs and datasets.
• Support submission-related activities and respond to programming and data-related queries from cross-functional and regulatory teams.
• Identify potential programming issues and proactively communicate risks, timelines, and solutions to project stakeholders.
• Coordinate programming activities across studies and ensure deliverables are completed within agreed timelines and quality standards.
• Provide technical guidance and mentorship to Statistical Programmers and other programming team members.
• Participate in client/project meetings and effectively communicate technical information to both technical and non-technical stakeholders.

• Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field
  .
• Strong experience in clinical trial statistical programming
  , preferably within a CRO, pharmaceutical, or biotechnology environment.
• Significant experience working on oncology clinical trials
  .
• Basic or working knowledge of R programming is preferred.
• Experience supporting regulatory submissions
• Strong proficiency in SAS programming
  , including Base SAS and relevant SAS procedures used for clinical trial reporting.
• Strong knowledge of CDISC standards
  , particularly SDTM and ADaM.
• Experience developing and validating TLFs for clinical trials.
• Experience working with complex clinical trial data and supporting statistical analyses.
• Ability to independently manage programming deliverables and lead study-level programming activities.
• Strong understanding of clinical development processes, including protocols, SAPs, datasets, TLFs, and clinical study reports.
• Excellent communication, organizational, problem-solving, and collaboration skills.

Clin Choice 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 mission drives our culture: to contribute to a healthier and safer world by accelerating the…