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Immediate Role SAS/Statistical Programmer/Developer
Chicago, IL
Chicago
IL
60701
Date
: Dec-18-20
2020-12-18
2021-12-18
Immediate Role SAS/Statistical Programmer/Developer
Chicago, IL
Dec-18-20
Work Authorization
US Citizen
GC
H1B
OPT EAD, L2 EAD, H4 EAD, TN EAD
Preferred Employment
Corp-Corp
W2-Permanent
W2-Contract
1099-Contract
Contract to Hire
Job Details
Experience
:
Senior, Midlevel
Rate/Salary ($)
:
$45/hour on C2C
Duration
:
12 months
Sp. Area
:
Data Warehousing/ETL
Sp. Skills
:
SAS
Consulting / Contract
CONTRACTOR
Required Skills
:
SAS, Clinical trials, SDTM, ADaM datasets, Merging, Baseline
Preferred Skills
:
Domain
:
HealthCare, Pharmaceuticals
Work Authorization
US Citizen
GC
OPT EAD, L2 EAD, H4 EAD, TN EAD
H1B
Preferred Employment
Corp-Corp
W2-Permanent
W2-Contract
1099-Contract
Contract to Hire
Job Details
Experience
:
Senior, Midlevel
Rate/Salary ($)
:
$45/hour on C2C
Duration
:
12 months
Sp. Area
:
Data Warehousing/ETL
Sp. Skills
:
SAS
Consulting / Contract
CONTRACTOR
Required Skills
:
SAS, Clinical trials, SDTM, ADaM datasets, Merging, Baseline
Preferred Skills
:
Domain
:
HealthCare, Pharmaceuticals
VLink Inc
South Windsor, CT
Post Resume to
View Contact Details &
Apply for Job
Job Description
:
Hi,
Hope you are doing great!
This is Shivali from VLink,
We have urgent requirement for SAS/Statistical Programmer for Chicago, IL location kindly have a look the requirement and reply me back with your updated resume.
Role: SAS/Statistical Programmer
Location: Chicago, IL
Duration: 6+ months
Interview type: Skype/Zoom
Job Description:
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.
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