Hello *Associate*,
Hope you are doing well
We have below requirement open. Please send me your genuine candidate on my
email ID m.vikri...@canopyone.com
*Title – Pharma Project Manager with Veeva RIM*
*Location – Charlotte NC*
Primary skill -
• Looking for a Pharma Project Manager within the regulatory affairs area,
Veeva RIM, Liquent Insight Manager in developing customized product for our
clients. The role is expected to drive technology discussions and analyze
the current landscape for gaps in addressing business needs. We needs a
motivated individual to challenge the status quo and provide thought
leadership/best practices to enhance our current services and technologies.
Strong PM candidates to manage their large integration and migration
projects within the regulatory affairs area. This is one of the complex
projects with the customer with lot of dependencies 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
Coordinates publishing efforts for all submissions to FDA and other global
health authorities. Creation of templates and profiles within InSight
Publisher according to RA and FDA specifications management of documents
within Documentum assembly of submissions through the use of established
templates and guidelines and XML backbone generation for electronic
submissions. Reviews to ensure accuracy and compliance of work produced.
Assesses impact of regulation changes to current work procedures and SOPs.
With the Manager, updates procedures and SOPs as appropriate and trains
personnel regarding all revisions.
--
*Thanks & Regards,*
*Thanks & Regards,*
*Vikritha Mustyala*
Tel: 703-831-8282 Ext. 253 <703-831-8282>9 .Fax: 7034392550
<703-867-7172>
Email: m.vikri...@canopyone.com Web: www.canopyone.com
<http://canopyone.com/>
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