Excellent knowledge of SAS computer package. * Excellent knowledge of industry standards, such as ... programmers.

60 Katalyst Principal Sas Programmer Jobs Hiring Near You
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
Excellent knowledge of SAS computer package * Excellent knowledge of industry standards, such as ... programmers
Statistical Programmer
Tampa, FL · On-site
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
Tampa, FL · On-site
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 ...
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.
SAS programming experience.
SAS programming experience.
SAS programming experience.
SAS programming experience.
Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures ... Implement and maintain standardized programming templates, macros, and tools to ensure consistency ...
Develop and validate SAS programs to generate analysis datasets, tables, listings, and figures ... Implement and maintain standardized programming templates, macros, and tools to ensure consistency ...
SAS programming experience.
SAS programming experience.
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
Bio Statistician
San Mateo, CA · On-site
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
Bio Statistician
San Mateo, CA · On-site
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
Statistician
Jersey City, NJ · On-site
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
Statistician
Jersey City, NJ · On-site
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
Principal Quality Engineer
Irvine, CA · On-site
The Principal Quality Engineer serves as a subject matter expert, partnering with cross-functional teams to ensure products meet customer, regulatory, and business requirements while driving ...
Principal Quality Engineer
Irvine, CA · On-site
The Principal Quality Engineer serves as a subject matter expert, partnering with cross-functional teams to ensure products meet customer, regulatory, and business requirements while driving ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
SAS Programming a MUST. Writes / reviews analysis plans and guide others on the team in its implementation. Defines appropriate methods and procedures for statistical analysis. Provides ...
Clinical Statistical Programmer
Princeton, NJ · On-site
Independently develop SAS/R programs to generate and validate datasets according to the Statistical ... Programming experience in SQL, JSON (Good to have). * Working experience with relational databases ...
Clinical Statistical Programmer
Princeton, NJ · On-site
Independently develop SAS/R programs to generate and validate datasets according to the Statistical ... Programming experience in SQL, JSON (Good to have). * Working experience with relational databases ...
We are seeking an experienced Principal Quality Engineer to lead quality engineering initiatives that ensure compliance, product quality, and continuous improvement across manufacturing and product ...
We are seeking an experienced Principal Quality Engineer to lead quality engineering initiatives that ensure compliance, product quality, and continuous improvement across manufacturing and product ...
Principal Quality Engineer
Milwaukee, WI · On-site
We are seeking an experienced Principal Quality Engineer to lead quality engineering initiatives that ensure compliance, product quality, and continuous improvement across manufacturing and product ...
New
Principal Quality Engineer
Milwaukee, WI · On-site
We are seeking an experienced Principal Quality Engineer to lead quality engineering initiatives that ensure compliance, product quality, and continuous improvement across manufacturing and product ...
New
We are seeking an experienced Principal Quality Engineer to provide technical leadership in quality engineering, regulatory compliance, and continuous improvement initiatives. This role is ...
We are seeking an experienced Principal Quality Engineer to provide technical leadership in quality engineering, regulatory compliance, and continuous improvement initiatives. This role is ...
As a Principal Supplier Engineer, you'll be the bridge between Boston Scientific Cardiac Diagnostics (CDx) cutting-edge design leading the integration of new and existing technologies into CDx ...
As a Principal Supplier Engineer, you'll be the bridge between Boston Scientific Cardiac Diagnostics (CDx) cutting-edge design leading the integration of new and existing technologies into CDx ...
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
The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing.
Responsibilities:
- Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc.
- Review CRF, database design, and edit check specs.
- Review study quality surveillance plan and monitor study conduct.
- Prepare and/or review SAP, TFL shells and specifications for variable derivation.
- Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables.
- Provide statistical and validation support for statistical analysis, analysis datasets and TFL.
- Review study report, manuscripts and other documents related to statistics.
- Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents.
- Perform other ad-hoc statistical activities as needed.
- Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming.
- Participates in monitoring CRO activities and reviewing CRO deliverables Other duties as assigned.
- Ph.D. or MS in Statistics or Biostatistics.
- Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience.
- Excellent knowledge of SAS computer package.
- Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines.
- Excellent organizational skills, time management, and ability to meet established deadlines.
- Excellent communication and interpersonal skills to effectively interface with others.
- Ability to work independently and problem-solve.
- Ability to provide leadership for the CRO statisticians and statistical programmers.