SAS Programmer III

  • location: Deerfield, IL
  • type: Contract
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job description

SAS Programmer III

job summary:
Description:

Essential Duties and Responsibilities.

- Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros.

- Collaborate with manager and other programmers through participation in formal and ad-hoc meetings.

- Prepare documentation on all production programming and validation activities; utilize best industry business practices and data standards for clinical data submissions to the FDA and other global regulatory agencies.

- Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for regulatory submissions.

- Independently program CDSIC SDTM, ADaM datasets.

- Map raw data to SDTM (Study data table model) in compliance with CDISC data model standards and create specifications for programming.

- Create ADaM Specifications & datasets from SDTM datasets per CDISC analysis data model standards and SAP.

- Program data displays (tables, listings, graphs) for inclusion in documents including publications, statistical reports, clinical study reports, and other regulatory documents, as required.

- Independently develop QC programs to validate peer programmers' SDTM, ADaM datasets, statistical tables, listings, and graphs

Qualifications.

- Demonstrate proficiency of programming skills.

- In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Strong Base SAS v9.2 or later; SAS-STAT, and SAS Macro experience.

- Ability to work on multiple tasks and prioritize tasks.

- Excellent analytical, problem-solving, organizational, time management, interpersonal and communication skills.

- QC experience.

Education and/or Experience.

- Bachelor's degree in Computer Science, Statistics, Engineering or related field plus 5 years of related experience.

- Required skills: create SDTM datasets from raw data according to CDISC standards (5 yrs); Create ADAM datasets from SDTM datasets according to CDISC analysis data model standards (3 yrs); Independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS datasets, spreadsheets, data listings, tables and graphical displays of clinical trials data (3 yrs);

- Prior experience working with Data Management on edit checks etc is preferred

 
location: Deerfield, Illinois
job type: Contract
work hours: 9am to 6pm
education: Bachelors
 
responsibilities:
Description:

Essential Duties and Responsibilities.

- Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros.

- Collaborate with manager and other programmers through participation in formal and ad-hoc meetings.

- Prepare documentation on all production programming and validation activities; utilize best industry business practices and data standards for clinical data submissions to the FDA and other global regulatory agencies.

- Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for regulatory submissions.

- Independently program CDSIC SDTM, ADaM datasets.

- Map raw data to SDTM (Study data table model) in compliance with CDISC data model standards and create specifications for programming.

- Create ADaM Specifications & datasets from SDTM datasets per CDISC analysis data model standards and SAP.

- Program data displays (tables, listings, graphs) for inclusion in documents including publications, statistical reports, clinical study reports, and other regulatory documents, as required.

- Independently develop QC programs to validate peer programmers' SDTM, ADaM datasets, statistical tables, listings, and graphs

Qualifications.

- Demonstrate proficiency of programming skills.

- In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Strong Base SAS v9.2 or later; SAS-STAT, and SAS Macro experience.

- Ability to work on multiple tasks and prioritize tasks.

- Excellent analytical, problem-solving, organizational, time management, interpersonal and communication skills.

- QC experience.

Education and/or Experience.

- Bachelor's degree in Computer Science, Statistics, Engineering or related field plus 5 years of related experience.

- Required skills: create SDTM datasets from raw data according to CDISC standards (5 yrs); Create ADAM datasets from SDTM datasets according to CDISC analysis data model standards (3 yrs); Independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS datasets, spreadsheets, data listings, tables and graphical displays of clinical trials data (3 yrs);

- Prior experience working with Data Management on edit checks etc is preferred

 
qualifications:
Description:

Essential Duties and Responsibilities.

- Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros.

- Collaborate with manager and other programmers through participation in formal and ad-hoc meetings.

- Prepare documentation on all production programming and validation activities; utilize best industry business practices and data standards for clinical data submissions to the FDA and other global regulatory agencies.

- Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for regulatory submissions.

- Independently program CDSIC SDTM, ADaM datasets.

- Map raw data to SDTM (Study data table model) in compliance with CDISC data model standards and create specifications for programming.

- Create ADaM Specifications & datasets from SDTM datasets per CDISC analysis data model standards and SAP.

- Program data displays (tables, listings, graphs) for inclusion in documents including publications, statistical reports, clinical study reports, and other regulatory documents, as required.

- Independently develop QC programs to validate peer programmers' SDTM, ADaM datasets, statistical tables, listings, and graphs

Qualifications.

- Demonstrate proficiency of programming skills.

- In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Strong Base SAS v9.2 or later; SAS-STAT, and SAS Macro experience.

- Ability to work on multiple tasks and prioritize tasks.

- Excellent analytical, problem-solving, organizational, time management, interpersonal and communication skills.

- QC experience.

Education and/or Experience.

- Bachelor's degree in Computer Science, Statistics, Engineering or related field plus 5 years of related experience.

- Required skills: create SDTM datasets from raw data according to CDISC standards (5 yrs); Create ADAM datasets from SDTM datasets according to CDISC analysis data model standards (3 yrs); Independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS datasets, spreadsheets, data listings, tables and graphical displays of clinical trials data (3 yrs);

- Prior experience working with Data Management on edit checks etc is preferred

 
skills: Description:

Essential Duties and Responsibilities.

- Develop programs that convert raw SAS datasets into standard format and improve existing programs by creating standard programs and macros.

- Collaborate with manager and other programmers through participation in formal and ad-hoc meetings.

- Prepare documentation on all production programming and validation activities; utilize best industry business practices and data standards for clinical data submissions to the FDA and other global regulatory agencies.

- Assist manager through contributions to continuous improvement by developing standard programs and macros that follow CDISC guidelines required for regulatory submissions.

- Independently program CDSIC SDTM, ADaM datasets.

- Map raw data to SDTM (Study data table model) in compliance with CDISC data model standards and create specifications for programming.

- Create ADaM Specifications & datasets from SDTM datasets per CDISC analysis data model standards and SAP.

- Program data displays (tables, listings, graphs) for inclusion in documents including publications, statistical reports, clinical study reports, and other regulatory documents, as required.

- Independently develop QC programs to validate peer programmers' SDTM, ADaM datasets, statistical tables, listings, and graphs

Qualifications.

- Demonstrate proficiency of programming skills.

- In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

- Strong Base SAS v9.2 or later; SAS-STAT, and SAS Macro experience.

- Ability to work on multiple tasks and prioritize tasks.

- Excellent analytical, problem-solving, organizational, time management, interpersonal and communication skills.

- QC experience.

Education and/or Experience.

- Bachelor's degree in Computer Science, Statistics, Engineering or related field plus 5 years of related experience.

- Required skills: create SDTM datasets from raw data according to CDISC standards (5 yrs); Create ADAM datasets from SDTM datasets according to CDISC analysis data model standards (3 yrs); Independently write, test, run, document, maintain and QC SAS programs and macros to generate SAS datasets, spreadsheets, data listings, tables and graphical displays of clinical trials data (3 yrs);

- Prior experience working with Data Management on edit checks etc is preferred


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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