Clinical SAS Programmer
Edison, NJ · On-site
Strong SAS programming and graphic programming skills * Able to guide the successful completion of major programs and projects. * Strong analytical and communication skills * Knowledge and experience ...

Edison, NJ · On-site
Strong SAS programming and graphic programming skills * Able to guide the successful completion of major programs and projects. * Strong analytical and communication skills * Knowledge and experience ...
Edison, NJ · On-site
Strong SAS programming and graphic programming skills * Able to guide the successful completion of major programs and projects. * Strong analytical and communication skills * Knowledge and experience ...
Boston, MA · On-site
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. * Programs quality checks for clinical study raw ...
Boston, MA · On-site
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. * Programs quality checks for clinical study raw ...
Minneapolis, MN · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Minneapolis, MN · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Boulder, CO · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Boulder, CO · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
* Looking for SDTM experts having in-depth knowledge of SAS programming(macro's). * Must have 10 yrs of exp in clinical domain. * Strong knowledge of SDTM. * Create advanced SAS macros, templates, and ...
* Looking for SDTM experts having in-depth knowledge of SAS programming(macro's). * Must have 10 yrs of exp in clinical domain. * Strong knowledge of SDTM. * Create advanced SAS macros, templates, and ...
Worcester, MA · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Worcester, MA · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Develop, implement and maintain SAS programming standards. * Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as ...
Develop, implement and maintain SAS programming standards. * Builds/tests programs for Data Validation, Derivation, and Data Reports to identify inconsistencies and support data review efforts, as ...
Strong SAS programming and graphic programming skills * Able to guide the successful completion of major programs and projects. * Strong analytical and communication skills * Knowledge and experience ...
Strong SAS programming and graphic programming skills * Able to guide the successful completion of major programs and projects. * Strong analytical and communication skills * Knowledge and experience ...
Newark, NJ · On-site
Create, maintain, and optimize SAS macros and utilities to enhance programming efficiency * Draft clear dataset specifications aligned with study protocols and analysis plans * Partner with ...
Newark, NJ · On-site
Create, maintain, and optimize SAS macros and utilities to enhance programming efficiency * Draft clear dataset specifications aligned with study protocols and analysis plans * Partner with ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. * Programs quality checks for clinical study raw ...
Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs. * Programs quality checks for clinical study raw ...
The Associate Clinical SAS Programmer/Junior Statistician will interact well with the Heartflow Clinical Research staff and collaborate effectively with principal investigators to ensure that data ...
The Associate Clinical SAS Programmer/Junior Statistician will interact well with the Heartflow Clinical Research staff and collaborate effectively with principal investigators to ensure that data ...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
* Looking for SDTM experts having in-depth knowledge of SAS programming(macro's). * Must have 10 yrs of exp in clinical domain. * Strong knowledge of SDTM. * Create advanced SAS macros, templates, and ...
* Looking for SDTM experts having in-depth knowledge of SAS programming(macro's). * Must have 10 yrs of exp in clinical domain. * Strong knowledge of SDTM. * Create advanced SAS macros, templates, and ...
As a Clinical SAS Programmer, you will be responsible for attending multi-disciplinary team meetings to represent the programming function. You will create or review and approve programming plans at ...
As a Clinical SAS Programmer, you will be responsible for attending multi-disciplinary team meetings to represent the programming function. You will create or review and approve programming plans at ...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office * Experience in ...
Create, maintain, and optimize SAS macros and utilities to enhance programming efficiency * Draft clear dataset specifications aligned with study protocols and analysis plans * Partner with ...
Create, maintain, and optimize SAS macros and utilities to enhance programming efficiency * Draft clear dataset specifications aligned with study protocols and analysis plans * Partner with ...
Provide statistical programming support for clinical trial data reporting under the general guidance of a biostatistician. * Develop SAS programs that generate tables, listings and figures and ...
Provide statistical programming support for clinical trial data reporting under the general guidance of a biostatistician. * Develop SAS programs that generate tables, listings and figures and ...
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Edison, NJ • On-site
Full-time
Re-posted 16 days ago