Responsibilities: Develop and maintain SAS programs to import, clean, and validate clinical trial data. Use R... and analysis plans. Generate tables, listings, and figures (TLFs) using SAS and R. Create and QC statistical outputs and clinical...
Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming... Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document...
experience in statistical programming with clinical trial data, particularly using SAS software. A strong team player who...
discipline. Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO... and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical...
), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies... and processes. Requirements: MS or PhD level Statistics. 5-6 years Pharmaceutical and/or CRO experience. SAS Programming...
most important research questions across clinical development, market access, and commercial use cases for our life sciences partners... with experience analysing real-world data (e.g., healthcare claims or electronic health records). Excellent programmer in R...
Responsibilities: Serve as the principal programming lead across multiple studies or a clinical program, ensuring..., and documentation of SDTM, ADaM, and TFLs in support of clinical study reports, regulatory submissions, publications, and ad-hoc...