HI

Please go through the requirements and let me know if you have any
consultants. Please send your best candidates with the following details 

 

Full Name 

Current Location 

Ready to relocate:

Contact Number

Email ID:

Rate: 

 

Location: Princeton, NJ

Duration: 6 Months

 

 

SAS PROGRAMMER:

 

Position Description

Support programming activities related to Clinical Study report, Regulatory
requests or ad-hoc requests for Early Development Programming Group.
Contribute to computer programming efforts for a clinical trial drug project
and to provide programming support for clinical trial data reporting and
regulatory submissions. Assumes protocol level and some project management
responsibility while supporting the Programming and Statistics lead. Able to
support multiple protocols independently and to contribute to integrated
summaries of efficacy and safety. Demonstrates strong SAS programming
skills; participates in protocol team and some project team interactions.
Builds successful relationships and seamless interfaces at the
protocol/project team level. Provides timely and effective communication to
the programming and statistics leads.

 

Requirements

 

Masters - 5 - 7 Years Experience Preferred

Strong knowledge SAS software, familiarity w/system development  

process & general computing as related to pharma development.

Knowledge clinical trials, pharma business & familiarity w/regulatory  

requirements.

Academic training should be in computing or scientific discipline.  

MS/A or equivalent (at least 2 years relevant experience  

w/demonstrated experience processing data from multiple protocols); or  

BS (at least 4 years relevant experience w/demonstrated experience  

processing data from multiple protocols.

 

 

Thank You and Have a nice day,

Sourav Das

 

Whitefield Technologies Inc. 

1001 Durham Ave. 

South Plainfield, NJ-07080

908-462-3112  Voice

480-772-4679 Fax

[email protected]

Yahoo ID: sourav_mssi

http://www.wftinc.net 

(we work with direct client)

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