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 ...
72 Katalyst Principal Sas Programmer Jobs Hiring Near You
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 ...
Clinical SAS Programmer
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 ...
Clinical SAS Programmer
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 ...
Sr. SAS Programmer
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 ...
Sr. SAS Programmer
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 ...
Sr. SAS Programmer
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 ...
Sr. SAS Programmer
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 ...
Sr. SAS Programmer
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 ...
Sr. SAS Programmer
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 ...
Clinical SAS Programmer
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 ...
Clinical SAS Programmer
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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Clinical SAS Programmer
Edison, NJ • On-site
Katalyst
Full-time
Re-posted 16 days ago
Job description
Responsibilities:
- Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget.
- Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences.
- Ensure all relevant deliverables including investigator brochures, publications, all regulatory submissions (SDTM/ADaM compliance), supporting documentation (define.xml, reviewer's guide, annotated CRFs) conforms to SOPs and to regulatory specifications.
- Conduct hands-on programming of deliverables including but not limited to IDMC meetings, DSUR, IB safety data review, Board meetings, Exploratory Analysis, etc.
- Ensure timely delivery of all statistical deliverables for each study assigned.
- Collaborate with study statistician and study team members to come up with timelines for statistical programming deliverables and other related action items.
- Follow departmental SOPs and processes for operational excellence.
- Lead statistical programming activities for regulatory submissions following CDISC standards.
- Review key study-related documents including but not limited to SAP, CRFs, DTS/DTA and data management plan.
- Take ownership for the completion of SDTM and ADAM specifications for assigned studies.
- Thorough understanding of clinical trial reporting process, as well as regulatory reporting requirements including electronic data submissions and CDISC implementation
- Thorough knowledge of SDTM/ADaM specifications and programming
- 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 in meeting regulatory guidelines, including both FDA and international regulatory agencies.
- Broad knowledge of medical/biological terminology in relevant therapeutic areas.
- Experience of leading both early and late-phase clinical studies including programming and validation of SDTM and ADaM data sets, tables, figures, and listings.
- Strong level SAS programmer with experience in delivering complex programming assignments, macros and analyses.
- Experience with BLA or NDA/sNDA to FDA/EMA is preferred. Experience with other major global health authority submission is a plus.
- Experience in management of CROs with respect to statistical programming.