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 ...
60 Katalyst Statistical Programmer Jobs Hiring Near You
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 ...
Statistical Programmer III
Raleigh, NC · On-site
Provide mentorship and support to more junior statistical programming staff * Collaborate with cross-functional stakeholders across our medical and scientific organization to execute and deliver on ...
Statistical Programmer III
Raleigh, NC · On-site
Provide mentorship and support to more junior statistical programming staff * Collaborate with cross-functional stakeholders across our medical and scientific organization to execute and deliver on ...
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 ...
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 ...
Interact with the project statistician and guides other programmers participating on a project team. * Experience with Pooled analysis, regulatory agencies requirements and e-submission experience.
Interact with the project statistician and guides other programmers participating on a project team. * Experience with Pooled analysis, regulatory agencies requirements and e-submission experience.
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 ...
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 ...
Act as primary programming contact for assigned studies, collaborating closely with statisticians, data managers, and medical writers in a fully remote, fast-paced environment. * Conduct independent ...
Act as primary programming contact for assigned studies, collaborating closely with statisticians, data managers, and medical writers in a fully remote, fast-paced environment. * Conduct independent ...
Statistical Programmer
Trumbull, CT · On-site
They also must have specific expertise in SDTM programming, have submissions experience, and MUST possess strong skill in graphing. * They need to be comfortable working as a strong independent ...
Statistical Programmer
Trumbull, CT · On-site
They also must have specific expertise in SDTM programming, have submissions experience, and MUST possess strong skill in graphing. * They need to be comfortable working as a strong independent ...
Lead statistical Programmer
Boston, MA · On-site
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role ...
Lead statistical Programmer
Boston, MA · On-site
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role ...
Generate and validate TLFs based on the Statistical Analysis Plan, TLF specifications, and industry best practices. * With minimal oversight, perform all programming activities and documentation for ...
Generate and validate TLFs based on the Statistical Analysis Plan, TLF specifications, and industry best practices. * With minimal oversight, perform all programming activities and documentation for ...
Act as primary programming contact for assigned studies, collaborating closely with statisticians, data managers, and medical writers in a fully remote, fast-paced environment. * Conduct independent ...
Act as primary programming contact for assigned studies, collaborating closely with statisticians, data managers, and medical writers in a fully remote, fast-paced environment. * Conduct independent ...
The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials * This role is key to implementing ...
The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials * This role is key to implementing ...
Senior Statistician
Edison, NJ · On-site
$88K - $108K/yr
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 ...
Senior Statistician
Edison, NJ · On-site
$88K - $108K/yr
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 ...
Clinical SAS Programmer
Edison, NJ · On-site
Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget.
Clinical SAS Programmer
Edison, NJ · On-site
Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget.
Clinical SAS Programmer
Boston, MA · On-site
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Provides programming support for adhoc analysis. * Identifies problems and develops global tools ...
Clinical SAS Programmer
Boston, MA · On-site
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Provides programming support for adhoc analysis. * Identifies problems and develops global tools ...
Clinical SAS Programmer
Jacksonville, FL · On-site
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Provides programming support for adhoc analysis * Identifies problems and develops global tools ...
Clinical SAS Programmer
Jacksonville, FL · On-site
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Provides programming support for adhoc analysis * Identifies problems and develops global tools ...
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Provides programming support for adhoc analysis * Identifies problems and develops global tools ...
Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for ... Provides programming support for adhoc analysis * Identifies problems and develops global tools ...
RWE Programmer
Avenel, NJ · Remote
Bachelor's degree in Computer Science, Statistics, Mathematics, or other subject with high statistical content. * Minimum four years SAS statistical programming experience. * Database programming ...
RWE Programmer
Avenel, NJ · Remote
Bachelor's degree in Computer Science, Statistics, Mathematics, or other subject with high statistical content. * Minimum four years SAS statistical programming experience. * Database programming ...
Sr. SAS Programmer
Minneapolis, MN · On-site
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming ...
Sr. SAS Programmer
Minneapolis, MN · On-site
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming ...
Sr. SAS Programmer
Worcester, MA · On-site
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming ...
Sr. SAS Programmer
Worcester, MA · On-site
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming ...
Sr. SAS Programmer
Boulder, CO · On-site
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming ...
Sr. SAS Programmer
Boulder, CO · On-site
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming ...
Katalyst Jobs Information
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 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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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:
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.