Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...

60 Katalyst Principal Sas Programmer Jobs Hiring Near You
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Proficient of SAS programming in a regulated clinical research environment.
Proficient of SAS programming in a regulated clinical research environment.
Statistical Programmer
Decatur, GA · On-site
Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group * At least 6 years of ...
Statistical Programmer
Decatur, GA · On-site
Advanced SAS macro programming experience is required for the development of global tools that will increase the efficiency and capacity of the Statistical Programming group * At least 6 years of ...
Senior Statistical Programmer
Lake Villa, IL · On-site
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible ... Independently develop, validate, document and troubleshoot SAS programs for the preparation of ...
Senior Statistical Programmer
Lake Villa, IL · On-site
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible ... Independently develop, validate, document and troubleshoot SAS programs for the preparation of ...
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible ... Independently develop, validate, document and troubleshoot SAS programs for the preparation of ...
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible ... Independently develop, validate, document and troubleshoot SAS programs for the preparation of ...
Sr. Statistical Programmer
Baltimore, MD · On-site
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible ... Independently develop, validate, document and troubleshoot SAS programs for the preparation of ...
Sr. Statistical Programmer
Baltimore, MD · On-site
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible ... Independently develop, validate, document and troubleshoot SAS programs for the preparation of ...
Clinical Data Manager
Mountain View, CA · On-site
Provide robust technical SAS programming expertise to support data management, including developing, validating, implementing, and maintaining data review listings, metrics, dashboards, and ...
Clinical Data Manager
Mountain View, CA · On-site
Provide robust technical SAS programming expertise to support data management, including developing, validating, implementing, and maintaining data review listings, metrics, dashboards, and ...
Sr. Statistical Programmer
Omaha, NE · On-site
A high level of SAS programming skills including SQL and macro development * Good knowledge and application of CDISC standards for SDTM and ADaM * Experience with Pinnacle21 and writing reviewer ...
Sr. Statistical Programmer
Omaha, NE · On-site
A high level of SAS programming skills including SQL and macro development * Good knowledge and application of CDISC standards for SDTM and ADaM * Experience with Pinnacle21 and writing reviewer ...
Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports) * Maintain complete and auditable documentation of all programming activities * Manage ...
Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports) * Maintain complete and auditable documentation of all programming activities * Manage ...
Lead Statistical Programmer
Boston, MA · On-site
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Lead Statistical Programmer
Boston, MA · On-site
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports) * Maintain complete and auditable documentation of all programming activities * Manage ...
Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports) * Maintain complete and auditable documentation of all programming activities * Manage ...
Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports) * Maintain complete and auditable documentation of all programming activities * Manage ...
Generate or perform quality control for SAS programs and other study documents (e.g., presentations and reports) * Maintain complete and auditable documentation of all programming activities * Manage ...
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Lead Statistical Programmer
San Francisco, CA · On-site
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
Lead Statistical Programmer
San Francisco, CA · On-site
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs ... Provide input into and negotiate statistical programming timelines. Ensure that timelines are ...
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing ... SAS/GRAPH a plus (SAS version 9 or higher). * Proficient in coding, debugging, and optimizing new ...
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing ... SAS/GRAPH a plus (SAS version 9 or higher). * Proficient in coding, debugging, and optimizing new ...
RWE 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 ...
RWE 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 ...
Develop SAS programs and statistical output for the management and reporting of clinical trial data ... Perform QC of the programming material prepared by external providers guaranteeing the output ...
Develop SAS programs and statistical output for the management and reporting of clinical trial data ... Perform QC of the programming material prepared by external providers guaranteeing the output ...
Statistical Programmer III
Raleigh, NC · On-site
... study principal investigator * Serve as subject matter expert on appropriate use cases for, and ... SDTM and ADaM models (using SAS) and related controlled terminologies, and knowledge or some ...
Statistical Programmer III
Raleigh, NC · On-site
... study principal investigator * Serve as subject matter expert on appropriate use cases for, and ... SDTM and ADaM models (using SAS) and related controlled terminologies, and knowledge or some ...
Excellent knowledge of SAS computer package * Excellent knowledge of industry standards, such as ... programmers
Excellent knowledge of SAS computer package * Excellent knowledge of industry standards, such as ... programmers
Katalyst Jobs Information
What is it like to work at Katalyst?
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 makes Katalyst an attractive place to work?
Job description
- Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
- Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
- Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts and other clinical publications; support systems to produce electronic regulatory submissions.
- Assist in establishing standardized programming procedures and work instructions.
- Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
- Develop and maintain clinical processing workflow systems.
- Assist in the development of client proposal documents.
- Provide leadership, project specific training, stakeholder management, external sponsor support, resource management, and project management for the required programming tasks supporting clinical trial activities.
- Provide input into and negotiate statistical programming timelines. Ensure that timelines are adhered to and coordinate and lead a statistical programming team to successful completion of a study within given timelines and budgets.
- Trained in sponsor SOPs and disseminate knowledge to project team members as appropriate.
- Provide input into, and mentor statistical programmers to provide input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers, etc.)
- records handling (e.g., Chapter 21 of the US Code of Federal Regulation - Part 11), and electronic submission of clinical data to agencies (e.g., e-CTD guidance and CDISC SDTM and ADaM standards)
- Assist in updating/writing PROMETRIKA standard operating procedures (SOPs)
- Develop tools in SAS for data analysis and reporting that comply with regulatory requirements.
- Develop specifications (e.g., metadata files), annotate CRFs and create SAS programs for the mapping of raw datasets to CDISC SDTM standards.
- Create define.xml files from metadata files for SDTM and ADaM
- Convert data received in other formats to SAS datasets.
- Must have expertise in SAS/BASE, SAS/STAT, and knowledge of SAS/CONNECT, SAS/ACCESS, SAS/MACRO, SAS/GRAPH, SQL, and ODS
- Knowledge of SDTM, ADaM, FDA and ICH guidance
- Understanding of Code of Federal Regulations (CFR) Title 21, Part 11 that covers the management of electronic records and electronic signatures in computer systems.
- Good organizational skills across individual projects and managing own and teamwork loads. Ability to organize, manage and complete multiple assignments with challenging timelines independently and effectively.
- Consistent experience as a lead statistical programmer on several concurrent projects
- Strong understanding of drug development, including knowledge of interfaces and interdependencies with other functions
- Strong mentoring skills as shown by leadership of projects and if applicable, junior team members.
- Excellent analytical skills
- Proven ability to learn new systems and function in an evolving technical environment.
- Ability to negotiate and influence to achieve results.
- Good presentation skills
- Good business awareness/business development skills (including financial awareness)
- Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
- Work effectively in a quality-focused environment.
- Knowledge of other programming languages and database management software packages is a plus.