Please find the specs of the requirement below; kindly send suitable
profiles to *srikanth.acha...@keyseries.us <srika...@logisofttechinc.com>
*Position: Clinical SAS Programmer*
*Location: Rockville, MD*
*Duration: 1 Year +*
*Interview: Phone, followed by face to face (No Skype)*
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
3. Resume has to *Vendor information with each of contract assignment
(for example: Pfizer/Aerotek, etc) and their work location of each
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
*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.
The group is very busy, and this is a pressing need because of increase
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
Thanks & Regards
Kindly submit your consultant profile to above Email ID. Email is the best
way to reach me out.
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