Clinical SAS Programmer
South Plainfield, NJ ยท On-site
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South Plainfield, NJ ยท On-site
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South Plainfield, NJ ยท On-site
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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 ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. Good understanding of worldwide regulatory requirements and clinical trial expertise ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. Good understanding of worldwide regulatory requirements and clinical trial expertise ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R.- * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R.- * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. * Good understanding of worldwide regulatory requirements and clinical trial ...
Interacts with Clinical, Regulatory, Statistical Programming, Data Management, and our company ... SAS and/or R. * Good understanding of worldwide regulatory requirements and clinical trial ...
Hartford, CT ยท On-site
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 ...
Hartford, CT ยท On-site
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 ...
Summary: * The senior/principal biostatisticians will be supporting Phase 2 or 3 studies and be ... Demonstrated experience in SAS programming with a specific emphasis on SAS procedures used in ...
Summary: * The senior/principal biostatisticians will be supporting Phase 2 or 3 studies and be ... Demonstrated experience in SAS programming with a specific emphasis on SAS procedures used in ...
The Principal Statistical Programmer will provide expert-level hands-on programming support and technical expertise to develop, maintain, validate, and execute SAS programs that access, visualize ...
The Principal Statistical Programmer will provide expert-level hands-on programming support and technical expertise to develop, maintain, validate, and execute SAS programs that access, visualize ...
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... Design and develop macros, applications, and other utilities to expedite JReview/SAS programming ...
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... Design and develop macros, applications, and other utilities to expedite JReview/SAS programming ...
Raleigh, NC ยท On-site +1
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... Design and develop macros, applications, and other utilities to expedite JReview/SAS programming ...
Raleigh, NC ยท On-site +1
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... Design and develop macros, applications, and other utilities to expedite JReview/SAS programming ...
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... Design and develop macros, applications, and other utilities to expedite JReview/SAS programming ...
Job Title: Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data ... Design and develop macros, applications, and other utilities to expedite JReview/SAS programming ...
Job Summary (Primary function) The Principal Biostatistical Programmer is responsible for ... Good SAS programming skills and attention to detail are essential. * Demonstrate knowledge of ...
Job Summary (Primary function) The Principal Biostatistical Programmer is responsible for ... Good SAS programming skills and attention to detail are essential. * Demonstrate knowledge of ...
Irvine, CA ยท On-site +1
The Principal Statistical Programmer is expected to work independently, deliver highquality ... Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure ...
Irvine, CA ยท On-site +1
The Principal Statistical Programmer is expected to work independently, deliver highquality ... Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure ...
Broomfield, CO ยท On-site
$140K - $205K/yr
Katalyst Description: Katalyst is an American technology company focused on dynamic space ... Drive cross-functional engineering efforts, balancing mission objectives, technical performance ...
Broomfield, CO ยท On-site
$140K - $205K/yr
Katalyst Description: Katalyst is an American technology company focused on dynamic space ... Drive cross-functional engineering efforts, balancing mission objectives, technical performance ...
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 ...
Irvine, CA ยท On-site +1
The Principal Statistical Programmer is expected to work independently, deliver high-quality ... Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure ...
Irvine, CA ยท On-site +1
The Principal Statistical Programmer is expected to work independently, deliver high-quality ... Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure ...
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 ...
$144K - $189K/yr
## (Senior) Principal Statistical ProgrammerApplylocations: Remote (US)time type: Full timeposted on ... Computer Skills:** โข Expert-level SAS programming with experience delivering complex programming ...
$144K - $189K/yr
## (Senior) Principal Statistical ProgrammerApplylocations: Remote (US)time type: Full timeposted on ... Computer Skills:** โข Expert-level SAS programming with experience delivering complex programming ...
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South Plainfield, NJ โข On-site
Full-time
Re-posted 6 days ago
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Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Scientific research and development services
51 - 200 Employees
South Plainfield, NJ, US