Pharma Project Manager within the regulatory affairs area, Veeva RIM, FIrstDoc
Cognizant is looking for a Pharma Project Manager within the regulatory affairs area, Veeva RIM,FIrstDoc
in developing customized product for our clients. The role isexpected to drive technology discussions and analyze the current landscape forgaps in addressing business needs. Cognizant needs a motivated individual tochallenge the status quo and provide thought leadership/best practices toenhance our current services and technologies. You mustbe legally authorized to work in the United States without the need foremployer sponsorship, now or at any time in the future. Key Qualifications:
Strong PM candidates (at least 10-15 yrs of Exp.) to manage theirlarge integration and migration projects within the regulatory affairs area.
Project team is span across USA, EU and Japan.
This is one of the complex projects with the customer with lot ofdependencies within different functions.
-Proficient in project management
-Responsible for handling multiple vendors, work streams.
-Responsible for project financials
-Responsible for project schedule
-Experience in GRA/ R&D/ LS domain CognizantInteractive
helps clients reinvent products, experiences and business modelsto create new value, differentiation and drive revenue in the digitaleconomy. We take an Experience centered approach
which useshuman insights to take ideas from vision to outcome and building end to endexperience led solutions that enables brands to transform their customer andemployee experiences using design, marketing and commerce capabilities About Cognizant
Headquartered in the U.S, Cognizant is a member of theS&P-500, Nasdaq-100, Fortune 200, and was recently ranked as the #1 FastestGrowing “All Star” by Fortune Magazine. Cognizant leverages a highly flexiblebusiness model, a seamless global delivery network, and deep domain expertiseto deliver to a long list of world-class companies that are leaders in theirown space.