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Listed below are the top 10 out of 11 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Madison, NJ
TechData is looking for Medical Writer, Statistician, Biomarker Biostatistician, SAS Programmer, Clinical database programmer, Clinical DataManagerfor our clients ...
TechData is looking for SAS Programmer, Biostatisticians for our pharmaceutical clients in Central and Northern NJ. Please see below requirements and send your ...
Our large Biopharma partner out of RTP, NC has an immediate need for 5 Clinical SAS Programmers. This position is a contract for 1 year with the option to be ...
Description The Principal Statistical Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and ...
Job Duties/Responsibilities Include: Provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, ...
Job Description: Provide programming input to CRF, SAP, analysis file specifications, and tables, figures, and listings (TFLs) shells. Write SAS programs to ...
Target Start Date: ASAP 12 month renewable contract REQUIRED: STRONG SAS and technical skills, must be professional Job Description: Sr. SAS Programmer needed ...
TechData is looking for SAS Programmer (Some positions can be telecommute, Biostatistician, Clinical Data Manager), Medical Information Specialist, Clinical ...
TechData is looking for Coding Manager, Clinical Data Analyst(SAS Programmer), Clinical Database Developer, Clinical Data Manager, Clinical Study Manager for ...
For your reference, we have included the original job posting below.
SAS Programmer
Job Number:
44648869
Company Name:
Sunrise Systems Inc
Job Location:
Madison, NJ US
Job Category:
Science & Biotech
SAS Programmer
Sorry Can't work with H1 Visa holders Description: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Leads programming efforts for multiple studies within Pfizer Consumer Healthcare. Reviews case report form (CRF) design. Programs edit checks from the Data Management Plan ...
