Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming... Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document...
of bachelor's degree in related science discipline. Minimum 6+ years' experience in SAS programming for phase I-IV clinical...Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing...
of bachelor's degree in related science discipline. Minimum 6+ years' experience in SAS programming for phase I-IV clinical...Responsibilities: Providing statistical programming and validation support for clinical study reports, overseeing...
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...
Responsibilities: The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming... support for clinical trials and contributing to the development of departmental standards. This includes developing...
Responsibilities: The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming... support for clinical trials and contributing to the development of departmental standards. This includes developing...
most important research questions across clinical development, market access, and commercial use cases for our life sciences partners... with experience analyzing 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...
, listings, and graphs from assigned clinical sources using SAS and/or R; leading development and maintenance of associated... in clinical research within Medical Device or Pharmaceuticals. Proficiency in Base SAS, SAS/STAT and SAS Macro language...
for CNS clinical trials, ensuring traceability from raw data through analysis outputs. Program and QC tables, listings..., and figures (TLFs) for interim and final clinical study reports, regulatory submissions, and client deliverables. Interpret study...