*Clinical SAS Programmer - 12+ months- Rockville, MD !!*

*Kindly reply to [email protected]*

*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
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.

Regards,
Sara Wilson - Technical Recruiter
Direct : 646-340-0603
[email protected]

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