Job Description :

Clinical PM with veeva

Primary skill - Prime

• 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.


Similar Jobs you may be interested in ..