Required || Statistical Programmer || Chicago, IL

08/05/20 10:52 AM

Greetings,

We have an opening for . Below are the requirement details, just go through it & if you feel interested, revert back to me with your updated resume Your earliest reply is highly appreciated.

Note: if you know of someone who may be a good fit, please forward this to them

Role: Statistical Programmer
Location: Chicago, IL
Work Authorization: USC & GC

 
Responsibilities:
Must have 5+ years of experience in programming.
• Demonstrated practical understanding of SDTM data sets creation and SAS programming concepts and techniques appropriate to the pharmaceutical industry.
• Demonstrated satisfactory ability to apply SAS programming knowledge to solve problems related to non-routine situations.
• Ensure internal consistency of output and assess consistency with other activities for the project, as applicable.
• Follow all department and project standards.
• Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and running all checking utilities.
• Responsible for ensuring peer review has been completed for all activities for the assigned projects.
• Ensure clarity, accuracy and consistency of case report forms (CRFs), database definitions, and specifications for analysis data sets for individual studies.
• Review for consistency across studies within a project.
• Ensure accuracy of database quality assurance checks and assess data accuracy and consistency.
• Develop database checks for routine and with supervision develop checks for non-routine situations.
• Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications.
• Responsible for the creation and accuracy of derivation programs for routine and with supervision create derivation programs for non-routine situations.
• Responsible for ensuring peer review has been completed for all derivation programs for assigned projects.
• Responsible for the creation and accuracy of submission data sets and analysis programs for routine situations and with supervision for non-routine situations.
• Responsible for the creation of data definition documents and TOCs.
• Responsible for ensuring peer review for all submission data sets and programs for the assigned projects.
 
Minimum Requirements:
• MS in Statistics, Computer Science or a related field with 5+ years of experience in efficacy programming.
• High degree of technical competence and communication ability, both oral and written.
• Competent in SAS programming and Macro development.
• Pharmaceutical or related industry experience with clinical trials, including familiarity with expectations of regulatory agencies, especially FDA and EMEA.

Thanks,
Next Level Business Services, Inc.
Consulting| Analytics| Staff Augmentation

VaishaliSharma
11340 Lakefield Drive Suite #200,
Johns Creek, GA, 30097
(904) 344-3291
vaishali.sharma@nlbservices.com
Web: www.nlbservices.com

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