- Merck & Co. (North Wales, PA)
- …in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPHDesigns and develops complex programming algorithmsAbility ... for regulatory submissions including analysis datasets, tables, listings, figures, SAS transport files and associated documentationEnsure programmatic traceability from… more
- Merck & Co. (Rahway, NJ)
- …expertise in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPHExperience with at least one other software ... Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environmentMS in Computer Science,… more
- Merck & Co. (North Wales, PA)
- …in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPHDesigns and develops complex programming algorithmsAbility ... Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science,… more
- Merck & Co. (North Wales, PA)
- …expertise in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPH; systems and database expertiseDesigns and ... Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer Science,… more
- Merck & Co. (North Wales, PA)
- …expertise in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPH; systems and database expertise Designs and ... and therapeutic area (TA) standards and following departmental standard operating procedures (SOPs) and good programming practice. Maintain and manage a project… more
- Merck & Co. (Rahway, NJ)
- …expertise in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPH; systems and database expertise.Experience leading ... Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment.MS in...Engineering or related field plus 7 or more years SAS programming experience in a clinical trial environment. Department… more
- Merck & Co. (Rahway, NJ)
- …group. The senior statistical programmer utilizes multiple programming languages including SAS and R to efficiently manipulate electronic healthcare databases to ... Sciences, Engineering or related analytical field plus 3 yrs experience in SAS and\or RBA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Merck & Co. (North Wales, PA)
- …all programs meet analysis requirements, internal standard operating procedures , and external regulatory requirementsEvaluates appropriateness of available software ... skills. --Solid knowledge of- statistical and data processing software eg SAS and/or R.-Solid understanding of worldwide regulatory requirements and clinical trial… more
- Genmab (NJ)
- …support teams (database set-up, completion guidelines, CRF designers, procedures , algorithm specifications and reporting requirements) Facilitates a culture ... experience in a pharmaceutical, biotech, CRO or Regulatory Agency Proficient in SAS programming, 6-8 years experience. Practical knowledge and experience using R to… more
- Merck (North Wales, PA)
- …expertise in SAS and clinical trial programming including data steps, procedures , SAS /MACRO, SAS /GRAPH + Designs and develops complex programming ... for regulatory submissions including analysis datasets, tables, listings, figures, SAS transport files and associated documentation + Ensure programmatic… more
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