Job Description :
Role: Project Manager - RIM/Regulatory
Location: Princeton, NJ
Duration: Long Term
Rate: DOE
Responsibilities:
-Project manager for multiple work-streams where part of the project will initially focus on: Defining of project scope, phasing strategy, definition of migration strategy, alignment with business process develop (potentially a separate project) to the formulation of a project plan and launch of execution. In conjunction with the IT PMO lead, incumbent will develop the program and governance structure, project/program communication plan, support planning for change management and will define the approach and plan to bring all of the project steps together into an implementation methodology. Responsible for oversight and delivery/maintenance of the project plan through to completion.
Qualifications:
- “Senior Project Manager” skills
-Experience preferences: Regulatory Domain, Veeva implementation.
-Experience requirements: Pharma/validation experience; Management of programs of several projects where defining the dependencies, constraints and defining a complete program structure where part of delivery; 3-5 years program/project management experience. Experience and skills in systems integration/migration, strong entrepreneurial skills, change management/communication and stakeholder engagement/management skills and experience. Experience with managing multiple vendors (providers) contract terms as well as integration of efforts across vendors into a single comprehensive project plan.