-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results... of SDTM and ADAM specifications for assigned studies. Requirements: Thorough understanding of clinical trial reporting...
-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results... of SDTM and ADAM specifications for assigned studies. Requirements: Thorough understanding of clinical trial reporting...
for clinical trials using the SAS system. Skilled in programming with SAS. Knowledge of additional programming languages... to clinical programming. Review draft clinical reports, journal articles, slide presentations, and other documents to assure...
Responsibilities: The Principal SAS Programmer independently leads programming activities for various purposes..., and patient profiles. In addition, the Principal SAS Programmer supports migration activities in the creation of Standard Data...
with the Illuminate platform in a clinical trial environment. Proficient in clinical data programming languages (e.g., SAS, R...Responsibilities: This position requires a solid understanding of clinical trials, data integration, and programming...
programming activities for clinical studies. This role requires strong SAS programming skills and expertise in CDISC standards... with cross-functional teams. Key Responsibilities: Serve as the lead statistical programmer on clinical studies, overseeing...
), and written reports to support clinical trial results using SAS. Create and review annotated CRF to STDM datasets. Produce...Responsibilities: Serves as lead programmer for assigned projects to provide statistical and programming support...
Job Description General Summary: The Senior Statistical Programmer II provides technical guidance on clinical... project teams. Work is performed on the design, development, and quality control process for SAS programs used to access...