Senior Statistical Programmer​/Analyst Consultant; solid oncology background

Position: Senior Statistical Programmer/Analyst Consultant (Need solid oncology background) Remote in US

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.

Key Responsibilities

• 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.

Required Qualifications

• 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…