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*Clinical SAS Programmer
Location: Rockville, MD
Duration: 12 Months
Interview: Phone, followed by face to face (No Skype)
Client: Otsuka / Covance*
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Required:
1.       Need 7+ years U.S. Pharmaceutical industry Clinical SAS
Programming experience (I will submit candidate with 6+ if I have to);
2.       Need to include VISA status – can only work with EAD/Permanent
Resident/US Citizen
3.       Resume has to Vendor information with each of contract assignment
(for example: Pfizer/Aerotek, etc) and their work location of each
assignment;
4.       Prefer EAST coast candidate – they will set up f2f interview right
after the technical phone screen.  It would be the best if they can be
available within 3 days notice;
5.       Need at least one reference check upon submitting resume, simply
include what reference said about their SAS programming skills onto the sub;
6.       Need few sentences write-up (candidates’ experiences vs. the
requirement below);

Description:
Must be extremely proficient in SAS Programming validation of Analysis data
sets, SDTMs, Tables and Listings.
Must have working experience with CDISC / SDTM / AdAM standards.
Experience working on NDA/IND filings (Big Plus)
Experience with Complex Efficacy Analysis
Experience with ISS/ISE/TLF
SAS/MACRO experience required
MS Statistics strongly preferred
 More than seven YEARS IN PHARMA INDUSTRY      .
Very strong communication skills needed.
Reliability is essential.

Other Info:
The group is very busy, and this is a pressing need because of increase
workload.
Primary work will be Validation of the Data Analysis for CSRs, ISS, Annual
reports , etc.
Consultant will be providing validation and conversion for a variety of
studies.

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Thanks and Regards,
Alvin Paul | Recruiting Manager
Office : 203-652-1444 Ext: 159
[email protected]
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