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Thread: HOT REQ - BUSINESS ANALYST - Pharmaceutical Drug Safety, Clinical Trials - Job id




HOT REQ - BUSINESS ANALYST - Pharmaceutical Drug Safety, Clinical Trials - Job id
country flaguser name
United States
2008-01-02 10:08:37
Hello,

Sunrise Systems Inc is an IT staff augmentation company and a direct vendor for various Fortune 1000 Companies. Kindly go through the following requirements and send me your resume in word format.
Please include your Candidate's complete name, location, availability, rate and contact  information in the body of the email along with a word copy of resume.

Please keep the subject line while responding to this email. If you have any more questions, feel free to give me a call.
Thanks!
--
Sincerely,
Dave Karlekar
Sunrise Systems
sunrisesys.com">davesunrisesys.com
www.sunrisesys.com
732-603-2200 X-216
732-603-2208 (Fax)
-----------------------------------------------
Job id - PZ28441BANJ
Client - Pharma Company
Title - Business Analyst - Pharmaceutical Drug Safety, Clinical Trials Exp
Location - Bridgewater, NJ
Duration - 12 Months
Rate - Open

In-person interview is required after phone screening.
Atleast 7+ years of experience is required. Business Analyst with 
Pharmaceutical Drug Safety, Clinical Trials Exp is REQUIRED. Experience with MS Office & VISIO is mandatory



TECHNICAL KNOWLEDGE
•	Experience with relational databases, web application,  and client-server concepts
•	Experience using productivity tools such as MS Office, Visio


FUNCTIONAL KNOWLEDGE 
	Experience in Pharmaceutical industry 
•	Experience in Drug Safety, Clinical Trials, and Pharmacovigilance and related systems
•	Experience with ARISg desirable

•	GxP knowledge and practices


RESPONSIBILITIES

•	Gather business, end-user and technical requirements for application/solution definitions 
Investigate and analyze alternatives and options.
•	Coordinate between Pfizer internal departments and external vendor organizations regarding system related activitiesLead design effort and guide team members through iterative design/development sessions 
•	Ensure and coordinate validation and quality related activities and deliverables  
•	Design and test application forms and scripts
•	Assure deliverables are consistent and compliant with company SOP’s and GxP
̶6;	Track status, provide regular status reports, and escalate issues

  




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