Patient Reported Outcomes • Health Economics and Outcomes Research • Clinical and Observational Research Design and Execution • Outcomes Regulatory Support • Statistics and Psychometrics
51 - 200
November 5
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, Lead SAS Programmer manages programming activities for SDTM domains. • Implements CDISC and client standards for clinical study data reporting.
• Minimum Education: BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 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 5 years’ experience with CDISC and SDTM compliance. • Skills: Excellent organizational skills and good verbal and written communication skills. Ability to work independently is required.
• Comprehensive and competitive total reward package. • World class employee benefits and supportive policies. • Wellbeing initiatives tailored to support you and your family.
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