Create and validate analysis data sets. * Create and validate patient profiles. * Program and ... Expertise in developing and using system-level macro programs. * Experience programming with SAS ...
Create and validate analysis data sets. * Create and validate patient profiles. * Program and ... Expertise in developing and using system-level macro programs. * Experience programming with SAS ...
... validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. * Programs for quality checks for clinical study raw data and report the ...
... validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. * Programs for quality checks for clinical study raw data and report the ...
... Perform SAS data manipulation and analysis programming -May work with medical writing, clinical ... Macro Facility, SAS/Graph, SAS / ODS, and SAS / Stat within a Windows operating system. Job Type ...
Quick apply
... Perform SAS data manipulation and analysis programming -May work with medical writing, clinical ... Macro Facility, SAS/Graph, SAS / ODS, and SAS / Stat within a Windows operating system. Job Type ...
Clinical SAS Programmer at Katalyst Healthcares and Life Sciences Lake Success, NY
Lake Success, NY · On-site
Clinical SAS Programmer - Katalyst Healthcares and Life Sciences. Lake Success, NY ... Contribute to the development of a macro library. * Work closely with data management to assure ...
Clinical SAS Programmer at Katalyst Healthcares and Life Sciences Lake Success, NY
Lake Success, NY · On-site
Clinical SAS Programmer - Katalyst Healthcares and Life Sciences. Lake Success, NY ... Contribute to the development of a macro library. * Work closely with data management to assure ...
... clinical trial data etc. Develop analysis plan and summarize the results into reports and ... SAS MACRO and SQL 4. Familiar with statistical models 5. Master degree in statistics or related ...
... clinical trial data etc. Develop analysis plan and summarize the results into reports and ... SAS MACRO and SQL 4. Familiar with statistical models 5. Master degree in statistics or related ...
SAS Programmer
Bethesda, MD · On-site
Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...
SAS Programmer
Bethesda, MD · On-site
Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...
SAS Programmer
Fort Detrick, MD · On-site
Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...
SAS Programmer
Fort Detrick, MD · On-site
Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...
SAS Programmer
Fort Detrick, MD · On-site
Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...
Quick apply
SAS Programmer
Fort Detrick, MD · On-site
Prepare, update, and maintain all versions of Statistical Programming Validation Plans, and all ... Develop statistical programming specifications (clinical data) and other statistical programs used ...
SAS Programmer
East Brunswick, NJ · On-site
Experience clarifying business and technical requirements with data requestors * Provides technical ... Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming.
SAS Programmer
East Brunswick, NJ · On-site
Experience clarifying business and technical requirements with data requestors * Provides technical ... Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming.
SAS Programmer
East Brunswick, NJ · On-site +1
Experience clarifying business and technical requirements with data requestors * Provides technical ... Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming.
SAS Programmer
East Brunswick, NJ · On-site +1
Experience clarifying business and technical requirements with data requestors * Provides technical ... Must Have experience in pharmaceutical or Bio-technology company with Clinical SAS Programming.
SAS Programmer III
South San Francisco, CA · On-site
$74/hr
... clinical study report (CSR). Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses. Years of Experience 5-7. Strong SAS Programming skills ...
SAS Programmer III
South San Francisco, CA · On-site
$74/hr
... clinical study report (CSR). Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses. Years of Experience 5-7. Strong SAS Programming skills ...
... Programmer) to support SAS modernization efforts by analyzing existing workflows and developing ... and validate SAS conversion complexity and feasibility • Develop and optimize data pipelines ...
... Programmer) to support SAS modernization efforts by analyzing existing workflows and developing ... and validate SAS conversion complexity and feasibility • Develop and optimize data pipelines ...
SAS Programmer III
San Francisco, CA · On-site
$79/hr
... clinical study report (CSR). Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses. Years of Experience 5-7. Additional Information $79/hr 18 ...
SAS Programmer III
San Francisco, CA · On-site
$79/hr
... clinical study report (CSR). Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses. Years of Experience 5-7. Additional Information $79/hr 18 ...
Performs and validates statistical analysis. * Independently reviews CSRs and performs data ... Strong SAS programming skills, with experience in SAS-Base, MACRO, STAT, and GRAPH. * Strong CDISC ...
Performs and validates statistical analysis. * Independently reviews CSRs and performs data ... Strong SAS programming skills, with experience in SAS-Base, MACRO, STAT, and GRAPH. * Strong CDISC ...
... data displays. Responsibilities : • Developing CDISC-compliant datasets and corresponding ... software validation procedures and test plans Qualifications : Required : • Minimum years of ...
... data displays. Responsibilities : • Developing CDISC-compliant datasets and corresponding ... software validation procedures and test plans Qualifications : Required : • Minimum years of ...
Develop, validate, and maintain SAS programs to create SDTM (Study Data Tabulation Model) and ADaM ... Advanced knowledge of Base SAS, SAS/STAT, SAS/GRAPH, SAS/Macro facility, and SQL. * CDISC Standards:
Develop, validate, and maintain SAS programs to create SDTM (Study Data Tabulation Model) and ADaM ... Advanced knowledge of Base SAS, SAS/STAT, SAS/GRAPH, SAS/Macro facility, and SQL. * CDISC Standards:
Senior/Principal Clinical Programmer
Raleigh, NC · On-site +1
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... JReview & SAS as part of standard data validation and reporting package for clinical studies.
Senior/Principal Clinical Programmer
Raleigh, NC · On-site +1
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... JReview & SAS as part of standard data validation and reporting package for clinical studies.
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Fulltime Position Works closely with other programmers, biostatisticians, and clinical data ... Imports and exports SAS data. * Assists data management group in performing data edit checks.
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
Fulltime Position Works closely with other programmers, biostatisticians, and clinical data ... Imports and exports SAS data. * Assists data management group in performing data edit checks.
... and validate SDTM and ADaM datasets in compliance with CDISC standards • Lead generation of ... programming and clinical data management • Strong expertise in: o SAS (Base, Macro, SQL, ODS ...
... and validate SDTM and ADaM datasets in compliance with CDISC standards • Lead generation of ... programming and clinical data management • Strong expertise in: o SAS (Base, Macro, SQL, ODS ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
... of clinical data for phase I-IV clinical development programs. Primary Responsibilities ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Sr. SAS Programmer - Pharma
San Diego, CA · On-site
... of clinical data for phase I-IV clinical development programs. Primary Responsibilities ... Experience in programming with the Statistical Analysis System (SAS) beyond classroom work is ...
Sas Programmer Clinical Data Validation Macro information
See salary details
$14.66 - $20.56
4% of jobs
$20.56 - $26.46
2% of jobs
$26.46 - $32.36
15% of jobs
$34.38 is the 25th percentile. Wages below this are outliers.
$32.36 - $38.26
12% of jobs
$38.26 - $44.17
14% of jobs
The median wage is $45.64 / hr.
$44.17 - $50.07
15% of jobs
$50.07 - $55.97
11% of jobs
$58.36 is the 75th percentile. Wages above this are outliers.
$55.97 - $61.87
8% of jobs
$61.87 - $67.77
9% of jobs
$67.77 - $73.67
3% of jobs
$73.67 - $79.57
7% of jobs
$14
$49
$79
How much do sas programmer clinical data validation macro jobs pay per hour?
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For Sas Programmer Clinical Data Validation Macro jobs, the most frequently searched job titles are:

SR. CLINICAL SAS PROGRAMMER at cGxPServe Indianapolis, IN
Indianapolis, IN • On-site
Other
Posted 22 days ago
Job description
- Perform data manipulation, analysis, and reporting of clinical trial data.
- Develop and maintain department/system-level macros.
- Create and review SDTM and Adam specifications.
- Create and validate SDTM data sets.
- Create and validate analysis data sets.
- Create and validate patient profiles.
- Program and generate tables, figures, and listings (TFLs).
- Validate and document SAS programs and outputs.
- Fulfil ad-hoc analysis requests.
- Provide other services.
- Bachelor's degree or higher, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or a related applicable field.
- Minimum of ten (10) years' SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
- Ability to create source and validation programs using SAS software for SDTM datasets, Adam datasets, and tables, figures, and listings (TFLs) for multiple studies/products.
- Experience integrating data across multiple studies or drug programs.
- Expertise in developing and using system-level macro programs.
- Experience programming with SAS/GTL.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
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