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...