Patient Reported Outcomes • Health Economics and Outcomes Research • Clinical and Observational Research Design and Execution • Outcomes Regulatory Support • Statistics and Psychometrics
51 - 200
Yesterday
Patient Reported Outcomes • Health Economics and Outcomes Research • Clinical and Observational Research Design and Execution • Outcomes Regulatory Support • Statistics and Psychometrics
51 - 200
• Working under the direction of the Technical Manager, Associate Director or Director, Statistical Programming, the SDTM SAS programmer supports the programming activities for the creation and validation of SDTM domains implementing CDISC and client standards for the reporting of clinical study data.
• Minimum Education: BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 3 years of SAS programming experience with clinical trial data. • Minimum Work Requirements: General knowledge of regulatory requirements and drug development process with a minimum of 3 years’ experience with CDISC and SDTM compliance. • Skills: Excellent organizational skills and good verbal and written communication skills. Ability to work independently is required.
Apply Now2 days ago
11 - 50
As an Autodesk Revit Plugin Developer, enhance workflows through advanced plugin design and implementation.
November 8
10,000+
Statistical Programmer II at Parexel providing expertise in clinical trial programming.
August 24
2 - 10
Develop and maintain WordPress websites for a leading Human Resources company.