Hi Associates,

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)*

* *

*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

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);


*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

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.

Thanks & Regards
Srikanth Acharya

Kindly submit your consultant profile to above Email ID. Email is the best
way to reach me out.

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