Support biometrics team with SDTM/ADaM programming for Phases 1-3 studies on exciting drug studies.

Statistical Programmer Consultant
in Healthcare + Life Sciences ContractJob Detail
Job Description
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
- ShareAustin: