Dear Business Partner,
Please send me the suitable resumes along with contact details and rate on c2c of your consultants for the following positions.
Please add vishal@swarkysolutions.com to your hotlist distribution list
SAS Developer
Round Lake, IL!
6+ month
RESPONSIBILITIES:
Assist manager in contributing to continuous improvement by developing standard programs and macros that follow CDISC guidelines
Assist manager in completing ad-hoc deliverables
Work independently and with Baxter personnel to complete deliverables
Develop Programs that convert raw SAS datasets to standard format and improvement by creating standard programs and macros
Program Data Displays (Tables, Listings, Graphs) for inclusion in documents including publications, stat reports, clinical study report and other regulatory documents as required.
Peer review of SAS Programming Code and deliverables (derived data, tables, listings graphs) as required
Work collaboratively with manager and other programmers by participating in formal and ad-hoc meetings
Prepare documentation on all production programming and validation activities
QUALIFICATIONS:
2+ years of SAS experience in the medical devices or pharmaceutical industry
On-site work, not a work from home position
Strong Base SAS and SAS Macro programming skills required
Programming experience with SDTM and ADAM required
Safety and Efficacy report programming required
Work with ODS, SAS-STAT procedures a plus
Creation of specifications for SDTM and ADAM a plus
Possess data analysis and problem solving skills
Experience with reading clinical trial data from EDC
Strong written and verbal communication skills required
SAS Developers Toolkit a plus
QC experience
Bachelors degree plus
--
-- Please send me the suitable resumes along with contact details and rate on c2c of your consultants for the following positions.
Please add vishal@swarkysolutions.com to your hotlist distribution list
SAS Developer
Round Lake, IL!
6+ month
RESPONSIBILITIES:
Assist manager in contributing to continuous improvement by developing standard programs and macros that follow CDISC guidelines
Assist manager in completing ad-hoc deliverables
Work independently and with Baxter personnel to complete deliverables
Develop Programs that convert raw SAS datasets to standard format and improvement by creating standard programs and macros
Program Data Displays (Tables, Listings, Graphs) for inclusion in documents including publications, stat reports, clinical study report and other regulatory documents as required.
Peer review of SAS Programming Code and deliverables (derived data, tables, listings graphs) as required
Work collaboratively with manager and other programmers by participating in formal and ad-hoc meetings
Prepare documentation on all production programming and validation activities
QUALIFICATIONS:
2+ years of SAS experience in the medical devices or pharmaceutical industry
On-site work, not a work from home position
Strong Base SAS and SAS Macro programming skills required
Programming experience with SDTM and ADAM required
Safety and Efficacy report programming required
Work with ODS, SAS-STAT procedures a plus
Creation of specifications for SDTM and ADAM a plus
Possess data analysis and problem solving skills
Experience with reading clinical trial data from EDC
Strong written and verbal communication skills required
SAS Developers Toolkit a plus
QC experience
Bachelors degree plus
--
Thanks &Regards,
Vishal,
Swarky Solutions Corporation |Plymouth, MN 55446|
Email : vishal@swarkysolutions.com
Web : http://www.swarkysolutions.com
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