The Principal SAS Programmer will be responsible for statistical programming for the client's clinical studies. * In this role, you will develop and validate SAS programs for data presentation ...
60 Katalyst Principal Sas Programmer Jobs Hiring Near You
The Principal SAS Programmer will be responsible for statistical programming for the client's clinical studies. * In this role, you will develop and validate SAS programs for data presentation ...
Principal SAS Programmer
Jersey City, NJ · On-site
The Principal SAS Programmer will be responsible for statistical programming for the client's clinical studies. * In this role, you will develop and validate SAS programs for data presentation ...
Principal SAS Programmer
Jersey City, NJ · On-site
The Principal SAS Programmer will be responsible for statistical programming for the client's clinical studies. * In this role, you will develop and validate SAS programs for data presentation ...
SAS Programmer
Hoboken, NJ · On-site
Are you prepared to integrate statistical concepts with SAS Programming efficiently and effectively ... Good Clinical Practice principals. * Good Programming Practice principals. * 21CFR Part 11 ...
SAS Programmer
Hoboken, NJ · On-site
Are you prepared to integrate statistical concepts with SAS Programming efficiently and effectively ... Good Clinical Practice principals. * Good Programming Practice principals. * 21CFR Part 11 ...
SAS Programmer
Boys Town, NE · On-site
Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. * Create source and validation programs using SAS software for ...
SAS Programmer
Boys Town, NE · On-site
Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. * Create source and validation programs using SAS software for ...
Clinical SAS Programmer
Boys Town, NE · 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
Boys Town, NE · 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 ...
Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. * Create source and validation programs using SAS software for ...
Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. * Create source and validation programs using SAS software for ...
Clinical SAS Programmer
Austin, TX · 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
Austin, TX · 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 ...
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 ...
Clinical SAS Programmer
Jacksonville, FL · 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
Jacksonville, FL · 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 ...
Requirements : * Bachelor's degree or equivalent and a minimum of 12+ years of SAS programming experience in the pharmaceutical/biotech industry. * Strong CDISC experience - ADaM expertise ...
Requirements : * Bachelor's degree or equivalent and a minimum of 12+ years of SAS programming experience in the pharmaceutical/biotech industry. * Strong CDISC experience - ADaM expertise ...
Clinical SAS Programmer
Addison, TX · On-site
Generate tables, listings, and figures (TLFs) using SAS and R. * Create and QC statistical outputs and clinical study reports for regulatory submissions. * Document programming activities and ensure ...
Clinical SAS Programmer
Addison, TX · On-site
Generate tables, listings, and figures (TLFs) using SAS and R. * Create and QC statistical outputs and clinical study reports for regulatory submissions. * Document programming activities and ensure ...
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 ...
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 ...
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 ...
Clinical SAS Programmer
Omaha, NE · 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
Omaha, NE · 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 ...
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
Irvine, CA · On-site
Minimum 6+ 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
Irvine, CA · On-site
Minimum 6+ 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 ...
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 ...
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 ...
Katalyst Jobs Information
What is a Principal SAS Programmer job?
A Principal SAS Programmer is a senior-level professional responsible for leading statistical programming activities in clinical trials or other data-driven industries. They design, develop, validate, and maintain complex SAS programs to analyze and report data, ensuring compliance with regulatory guidelines. Additionally, they collaborate with biostatisticians, data managers, and clinical teams to support study objectives. Their role often includes mentoring junior programmers and optimizing programming workflows for efficiency and accuracy.
What are the key skills and qualifications needed to thrive in the Principal Sas Programmer position, and why are they important?
To thrive as a Principal SAS Programmer, you need advanced expertise in SAS programming, statistical analysis, and clinical data management, often gained through a degree in statistics, computer science, or a related field. Familiarity with industry-standard tools like SAS Base, SAS Macro, and regulatory submission standards such as CDISC (SDTM, ADaM), as well as relevant certifications, is highly valued. Leadership, problem-solving, and effective communication are essential soft skills for managing projects and collaborating with cross-functional teams. These competencies are crucial for ensuring data integrity, regulatory compliance, and the successful delivery of complex clinical projects.
What are the typical responsibilities and day-to-day tasks for a Principal SAS Programmer?
As a Principal SAS Programmer, your daily tasks often include developing and validating statistical programs, overseeing the creation of datasets, tables, listings, and figures (TLFs) for clinical studies, and ensuring data quality and compliance with regulatory standards. You’ll collaborate with statisticians, data managers, and clinical teams to understand study requirements and deadlines. Additionally, you may mentor junior programmers, provide programming guidance, and help resolve technical challenges within the team. This role offers a mix of independent programming work and cross-departmental collaboration, making it both technically challenging and highly impactful within the organization.
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.
What are the most popular jobs at Katalyst?
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Job description
Responsibilities:
- The Principal SAS Programmer will be responsible for statistical programming for the client's clinical studies.
- In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members.
- Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment.
- Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I-III clinical studies.
- Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS.
- Create and review annotated CRF to STDM datasets.
- Produce and maintain technical programming specification documents.
- Lead and actively participate in client and project review meetings.
- Communicate with clients regarding study protocol or statistical analysis issues.
- Validate statistical deliverables and ensure that appropriate statistical methods are utilized.
- Ensure adherence to industry standards and regulatory requirements.
- Facilitate the development and application of adequate statistical methods in clinical research.
- PhD or MS degree in Statistics, Biostatistics or related field.
- 5+ years of relevant work experience in CRO, biotech, pharmaceutical, or life sciences industry.
- Familiarity with clinical trial design and analysis activities and knowledge of regulatory guidelines (FDA/EMA, ICH/GCP).
- Experience with NDA/BLA submission activities.
- Experience in statistical programs such as Statistical Analysis System (SAS), CDISC and SDTM.
- Maintain awareness of industry standards, regulatory requirements, departmental guidelines, and Standard Operating Procedures (SOP's).
- Excellent organizational skills, time management, ability to prioritize workload, and meet deadlines.
- Excellent communication and interpersonal skills to effectively interact with others.