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Saturday, April 20, 2013

{SAP JOBS USA:116835} CONFIRM RATES, ASAP -- $55/Hr. on C2C -- " Sr. Business Systems Analyst / Validation Lead " @ South San Francisco, CA

Greetings Partners,
 
This is Tushar (Tim) from Droisys Inc. Hope you are doing well.

Kindly let me know if you have available candidates for the position mentioned below. Kindly respond me back with your consultant's Updated Resume, along with Hourly Rate Confirmation & Full-Contact Details, at your earliest convenience.
 
Position          :          Sr. Business Systems Analyst/Validation Lead
Location          :         
South San Francisco, CA
Duration         :          Long Term
Rate                :          $55/Hr. on C2C           

                     
Need from Pharma background with experience in GCP & GMP

 

Job Description:

·       This contractor will fill in a systems analyst/solution lifecycle manager for projects within the Product Development Informatics group supporting Global Product Development Clinical Operations, Biometrics and Clinical Sciences business functions.   This role includes working on major cross-functional system initiatives.

·       He/she will analyze the customer needs, assess risks, perform impact analysis, define solutions, document requirements and functional specifications, work with the development team, develop validation and testing strategies and plans and validation/test summary reports.

·       He/she will participate in the review of system change requests and enhancements.

·       He/she will be asked to help in creating project plans with regards to planning tasks and timelines related to his/her job assignment.

 

Education:

·       Bachelor's degree in Computer Science, Informatics, Life Sciences or a related discipline

·       A minimum of five years' work experience as an IT business analyst, systems analyst combined with software validation/quality assurance experience with knowledge of pharmaceutical industry and processes

·       A good understanding of the principles of software validation in regulated industries is a plus, including 21 CFR Part 11, PDA 18, related FDA guidelines and regulations, as well as ICH GCP guidelines.

·       Knowledge of clinical trial management systems (CTMS), clinical trial portals (CTP), Electronic Data Capture (EDC) systems, document management systems such as Livelink, Microsoft Sharepoint, SAS, R-Software, Secure Data Exchange a plus

 


Kindly include the below details in your reply, ASAP :
 
Candidate Full name         :
Contact number                :
Alternate Number              :
Email ID                           :
Current location                :
Work visa authorization     :                                                                                                                                   
Available time to join        :
Years of Experience in IT  :
Total US on-site Exp.       :
Full Education Details       :                                         
 
 
Note : Pls add your Id to our Mailing List. Click on below link
http://tiny.cc/huggow
 
 
Warm Regards,
Tushar (T i m)
 
Cell : 408-459-2546
Work:408-874-8333 ext277
E-Mail : tim@droisys.com , http://www.droisys.com





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