Spectraforce Technologies
Clinical Statistical Programmer III
Spectraforce Technologies, Jersey City, New Jersey, United States, 07390
Clinical Statistical Programmer
III
1+ months (c an be extended up to 6 months.)
Remote
Qualifications
:
Minimum Education: B.S. or equivalent in computer science, mathematics, or life science.
Required Experience:
* A minimum of 5 years of relevant clinical research programming experience, 3 years specifically in the pharmaceutical industry.
Desired background and experience:
* Demonstrable experience/expertise in analysis and reporting of phase I-IV clinical trial data.
* Demonstrable experience/expertise using SAS/Base and SAS/Stat.
* Demonstrable experience/expertise using CDISC standards: CDASH, SDTM, ADaM, DEFINE-XML, Controlled Terminology.
* Demonstrable proficiency in MS Office (Outlook, Word, Excel, PowerPoint).
Responsibilities:
POSITION SUMMARY
* Provide programming support for study deliverables as assigned, ensuring that timelines are met and expected quality is attained.
* Liaise with Data Management and Biostatistics for database and dataset specifications, timelines, and quality requirements.
* Create and validate SDTM and ADaM datasets and associated submission deliverables in compliance with published industry standards and project/study specific requirements.
* Create and validate TFL output in compliance with study specific requirements.
* Receive, import, and verify the structure of external data.
* Create and maintain supporting documentation.
Maintain professional currency through:
* Demonstrable expertise in SAS analysis and reporting programming.
* Demonstrable expertise with CDISC CDASH, SDTM, ADaM, DEFINE-XML, and/or controlled terminology.
* Perform other duties as assigned.
III
1+ months (c an be extended up to 6 months.)
Remote
Qualifications
:
Minimum Education: B.S. or equivalent in computer science, mathematics, or life science.
Required Experience:
* A minimum of 5 years of relevant clinical research programming experience, 3 years specifically in the pharmaceutical industry.
Desired background and experience:
* Demonstrable experience/expertise in analysis and reporting of phase I-IV clinical trial data.
* Demonstrable experience/expertise using SAS/Base and SAS/Stat.
* Demonstrable experience/expertise using CDISC standards: CDASH, SDTM, ADaM, DEFINE-XML, Controlled Terminology.
* Demonstrable proficiency in MS Office (Outlook, Word, Excel, PowerPoint).
Responsibilities:
POSITION SUMMARY
* Provide programming support for study deliverables as assigned, ensuring that timelines are met and expected quality is attained.
* Liaise with Data Management and Biostatistics for database and dataset specifications, timelines, and quality requirements.
* Create and validate SDTM and ADaM datasets and associated submission deliverables in compliance with published industry standards and project/study specific requirements.
* Create and validate TFL output in compliance with study specific requirements.
* Receive, import, and verify the structure of external data.
* Create and maintain supporting documentation.
Maintain professional currency through:
* Demonstrable expertise in SAS analysis and reporting programming.
* Demonstrable expertise with CDISC CDASH, SDTM, ADaM, DEFINE-XML, and/or controlled terminology.
* Perform other duties as assigned.