Contribute to the development and maintenance of SAS macro programs and departmental programming standards. * Participate in SOP and work instruction development, including program validation and ...
60 Katalyst Principal Sas Programmer Jobs Hiring Near You
Contribute to the development and maintenance of SAS macro programs and departmental programming standards. * Participate in SOP and work instruction development, including program validation and ...
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 ...
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 ...
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 ...
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 ...
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 ...
Clinical SAS Programmer
Chicago, IL · 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
Chicago, IL · 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
Seattle, WA · 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
Seattle, WA · 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 ...
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 ...
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 ...
Sr. SAS Programmer
Avenel, NJ · Remote
Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various ...
Sr. SAS Programmer
Avenel, NJ · Remote
Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various ...
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 ...
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 ...
This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs * Develop and validate SAS programs ...
This role is key to implementing programming standards and supporting the standardization of CDISC-compliant datasets (e.g., SDTM, ADaM) across clinical programs * Develop and validate SAS programs ...
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Imports and exports SAS data. * Assists data management group in performing data edit checks ... Minimum of 10+ years of statistical programming experience in the life science industry and ...
Imports and exports SAS data. * Assists data management group in performing data edit checks ... Minimum of 10+ years of statistical programming experience in the life science industry and ...
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. * The successful candidate will work closely with the Biostatisticians, Data ...
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. * The successful candidate will work closely with the Biostatisticians, Data ...
Provides SAS programming support to all clinical studies. * Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables. * Provide statistical programming ...
Provides SAS programming support to all clinical studies. * Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables. * Provide statistical programming ...
Katalyst Jobs Information
What is it like to work at Katalyst?
Katalyst appears to be a collaborative and innovative company that values creativity and teamwork, fostering an environment where employees can share ideas and work together to achieve common goals.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
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Job description
Responsibilities:
- Develop, maintain, and execute SAS programs to support external data transfers, including validation against vendor transfer specifications.
- Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) in accordance with study timelines.
- Perform peer review of DRLs and data reconciliation reports.
- Monitor automated job logs and resolve issues as needed.
- Retrieve and post external vendor data using sFTP/FTP clients and vendor portals.
- Collaborate with data managers, statistical programmers, biostatistics, and clinical operations to support data cleaning and integrity activities.
- Contribute to the development and maintenance of SAS macro programs and departmental programming standards.
- Participate in SOP and work instruction development, including program validation and documentation.
- Provide guidance and support to junior members of the data programming team.
Requirements:
- Bachelor's or Master's degree in a relevant field or equivalent experience.
- 7+ years of clinical data programming experience, with a minimum of 5 years in oncology.
- Hands-on experience across Phase I, II, and III oncology trials.
- Proficiency in SAS; working knowledge of Medidata Rave, Business Objects, and Crystal Reports.
- Familiarity with CDISC, 21 CFR Part 11, ICH, and GCP guidelines.
- Experience with sFTP/FTP tools and vendor data portals.