This is a Senior level role, Senior Manager.
You must have Healthcare experience along with the MDM implementation, ideally from a consulting environment.

Summary description:
The role requires a strong business and technical aptitude in defining and implementing a large scale Master Data Management (MDM) Program for a Federal drug regulatory agency.
Experience with Pharmaceutical data domains and drug regulatory review processes is strongly desired.
The role also requires senior level program/project management experience, Informatica MDM (formerly Siperian MDM) technical expertise, data governance, business subject matter expertise around Pharmaceutical data sets, and customer relationship management (pharmaceutical regulatory review experts).
Responsibilities include working with multiple Programs.
This lead role includes collaboration with other Programs to define business rules for processing customer data, partnering with IT Shared Services, Application Services Vendors and Data Steward's to execute projects in MDM space.
The MDM program is required to support process improvement and technology solution implementations that will utilize the Master Data in downstream use.Contact Gary@CantignyGroup.com