Clinical SAS Programmer

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all relevant deliverables including investigator brochures, publications, all regulatory submissions (

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's and . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as a Senior Director, Clinical Data Standard

Job Description: The senior programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various data sources with a careful eye for outliers and errors. Prior experience building patient cohorts and evaluatin

Role: SAS Programmer Pharma/Biotech exp must Remote! Location: USA, Remote Visa: Any visa Job Description: This is a RWE Programmer position. The top 3 skills are: RWE/HEOR experience: Claims, EHR, EMR data. Not ETL or building dashboards or clinical trial data. This is purely a RWE position SAS Programming skills Pharma/Biotech experience. Insurance experience is ok and government experience isnt what we are looking for The senior programmer position will be responsible for manipulati