Statistical Programmer
North Chicago, IL · On-site
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. * The successful candidate will work closely with the Biostatisticians, Data ...
60 Katalyst Statistical Programmer Jobs Hiring Near You
Statistical Programmer
North Chicago, IL · On-site
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. * The successful candidate will work closely with the Biostatisticians, Data ...
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 ...
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 ...
Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I - IV clinical trials, integrated clinical summaries, responses to ...
Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I - IV clinical trials, integrated clinical summaries, responses to ...
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
Sr.Statistical Programmer
Boulder, CO · On-site
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
Sr.Statistical Programmer
Boulder, CO · On-site
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
Maintains a basic understanding of relevant industry trends in standards implementation, clinical statistical programming, and ophthalmology * Provides technical consultation and collaborates with ...
Maintains a basic understanding of relevant industry trends in standards implementation, clinical statistical programming, and ophthalmology * Provides technical consultation and collaborates with ...
Lead Statistical Programmer
Tarrytown, NY · On-site
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 ...
Lead Statistical Programmer
Tarrytown, NY · On-site
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 ...
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
The Senior Statistical Programmer will serve as the lead statistical programmer and is responsible for statistical programming activities such as designing, developing, validating, updating, and ...
Lead Statistical Programmer
Boston, MA · On-site
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 ...
Lead Statistical Programmer
Boston, MA · On-site
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 ...
Senior Statistical Programmer
Boulder, CO · On-site
Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...
Senior Statistical Programmer
Boulder, CO · On-site
Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...
Sr. Statistical Programmer
Cincinnati, OH · On-site
Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...
Sr. Statistical Programmer
Cincinnati, OH · On-site
Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...
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 ...
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 ...
Senior Statistical Programmer
Austin, TX · On-site
Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...
Senior Statistical Programmer
Austin, TX · On-site
Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time deliverables within budget * Generate, validate, and/or ...
Support statisticians in the preparation and/or review and QC of statistical package for FDA submissions * Perform QC of the programming material prepared by external providers guaranteeing the ...
Support statisticians in the preparation and/or review and QC of statistical package for FDA submissions * Perform QC of the programming material prepared by external providers guaranteeing the ...
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 ...
Statistical Programmer I
Omaha, NE · On-site
Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD). * Provides primary programming and QC support for any internally ...
Statistical Programmer I
Omaha, NE · On-site
Provide statistical programming support for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD). * Provides primary programming and QC support for any internally ...
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 ...
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 ...
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 ...
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 ...
Lead Statistical Programmer
Newark, NJ · On-site
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 ...
Lead Statistical Programmer
Newark, NJ · On-site
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 ...
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 ...
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
Responsibilities:
Requirements:
- The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
- The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting
- Develop and validate SAS programs to support clinical trial data analysis and reporting
- Create, maintain, and document SAS programming standards and procedures
- Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
- Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
- The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry
- Prepare datasets for analysis, including merging and cleaning data from various sources
- Prepare and review tables, listings, and figures for clinical study reports
- Ensure compliance with regulatory requirements and guidelines
- Keep up to date with new SAS programming methods and software, as well as regulatory guidance
Requirements:
- Bachelor's Degree in statistics, computer science, or a similar quantitative field
- 4+ years of clinical statistical programming experience within the pharmaceutical or related industry
- Proficiency in SAS programming
- Knowledge of CDISC data standards
- Strong attention to detail and ability to work independently
- Excellent problem-solving skills
- Excellent verbal and written communication skills
- Knowledge of regulatory requirements for clinical trials and drug development
- Ability to work in a team environment and collaborate effectively with other stakeholders