Statistical Programmer Consultant

Remote, TX 00000

Posted: 06/11/2025 Employment Type: Contract Job Category: Biostatistics Job Number: 620349 Is job remote?: Yes Country: United States

Job Description


JOB DESCRIPTION
Position Summary
Working with the Biometrics staff, the Statistical Programmer Consultant provides programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work. Provides timely support to the project team on all statistical programming matters according to the project strategy.  Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables. Identifies and communicates changes in project requirements that may affect key deliverables.

Responsibilities
·       Involved in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs
·       Creates and reviews annotated CRF to SDTM datasets
·       Provides support in balancing conflicting priorities, promoting communication and adequate information flow to motivate, encourage and align people with the company' s strategic objectives
·       Functions as a positive role model for setting high expectations for quality, creativity and project ownership
·       Works collaboratively with Clinical Operations, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting
·       Provides technical input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers)
·       Works with Biometrics and other functions for the development and maintenance of the data review and reporting tools, and any other statistical applications as appropriate
·       Involved with the strategy for process improvement
·       Identifies new tools to increase efficiency and quality


Requirements:
·        Master's Degree in Statistics, Computer Science, Mathematics, Engineering or related discipline
·       Minimum of 1-5 years of clinical trial programming experience in the biotechnology, pharmaceutical or health related industry
·       Advanced SAS programming skill s and experience in other statistical software, such as R and S-Plus
·       Experience and in-depth knowledge in CDISC including SDTM, ADaM, and controlled terminologies
·       Self-directed, technically strong, and a recognized leader maintaining a strategic prospective with regards to statistical programming processes, management of statistical programing projects
·       Excellent organizational skills and ability to prioritize  tasks









Pay Rate Range: $60-75/hr depending on experience 
Apply Online

Send an email reminder to:

Share This Job:

Related Jobs:

Login to save this search and get notified of similar positions.