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Clinical Data Solution
Sugar Hill, GA 30518
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Independently carry analysis of data collected during clinical trial and ability to write report based on the result of analysis.
Syntactx
New York, NY 10007 (Financial District area)
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Manage and analyze large clinical trial datasets. Ad hoc programming for clinical, data management and safety departments. Skilled use of computer technology.
Tech-Observer
Woodcliff Lake, NJ
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Clinical studies and clinical trials: *Providing statistical programming and validation support for clinical study reports, and publications.
As required, oversees program level clinical programming operations by providing supervision for a team of clinical programmers. Travel Yes, 25 % of the Time.
Katalyst HealthCares & Life Sciences
Rockville, MD
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Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.
Robarts Clinical Trials
San Diego, CA 92121
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The SAS Programmer is responsible for developing and executing biostatistical (SAS) and data management related programs, processing data from various sources…
Katalyst Healthcares & Life Sciences
Rockville, MD 20849 +18 locations
Assist clinical statisticians in the development and review of statistical analysis plans (SAPs) and SAS programming specifications.
Pharma RI International
Woodcliff Lake, NJ
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Define and create ad-hoc reports for clinical research teams. Develop and validate SAS programs for clinical trials, including phase II & III studies.
Silver Spring, MD
Familiarity with clinical data analyses, particularly concerning clinical pharmacology study results. Pharmacokinetics analysis of clinical pharmacology…
Syntactx
New York, NY 10007 (Financial District area)
Easily applyResponsive employer
Manage and analyze large clinical trial datasets. Ad hoc programming for clinical, data management and safety departments. Skilled use of computer technology.
RR SOLUTIONS
Parsippany, NJ
Provide clinical programming expertise & hands on suppt to clinical projects across multiple therapeutics areas.
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GCP, ISO 14155, ICH and other regulatory environments pertaining to clinical data and clinical data management. This is a Fulltime role with MaxisIT.
RGAL
North Chicago, IL
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Phase 1-3 clinical trials: 8+ Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry.
Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training…
The American College of Radiology
Philadelphia, PA
Experience in a multi-modality clinical trials group or research team a plus. The American College of Radiology (www.ACR.org), a professional association for…
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