Katalyst
Katalyst

60 Katalyst Principal Sas Programmer Jobs Hiring Near You

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 ...

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 ...

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 ...

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 ...

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Katalyst Jobs Information

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What makes Katalyst an attractive place to work?

Katalyst is a forward-thinking company that has established itself as a leader in its industry, known for its commitment to innovation and customer satisfaction. The company's work environment is characterized by a collaborative and dynamic atmosphere, where employees are encouraged to share ideas and work together to drive progress. Joining Katalyst offers opportunities for professional growth and development, as well as the chance to contribute to meaningful projects that can have a lasting impact.
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Infographic showing various Principal Sas Programmer job openings at Katalyst in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.

Senior Principal Statistical Programmer

Katalyst

Newark, NJ

Full-time

Re-posted 3 days ago


Job description

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.
Requirements:
  • 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.