In this role, you will deliver consistent communication and educates employees on administrative and/or technical operations in order to maximize performance and to ensure understanding of compliance with external regulatory bodies as well as Company goals and policies.
In this role, the selected candidate will be responsible for accurate and timely processing of contract bookings including audit of contract file by verifying the accuracy of all transaction details including equipment cost and location.
In this role, the selected candidate will oversee all digital advertising campaigns including, but not limited to, front-end research, order entry, creative management, campaign optimization, and post-sale activity.
In this role, you will be responsible for assembly, electronic publishing and filing of global regulatory submissions. This includes technical writing and project management of complex submissions (e.g., drug/device combination, original PMA submissions, etc.); compiling timely and accurate information for internal and external customers per deadlines.
This role also provides first level support for BU users of our RIM systems. This position may serve as project management officer within the SH team, as well as technology liaison between the Structural Heart Regulatory Operations team, MDT IT, and Corporate Regulatory Operations.
In this role, you will direct quality review of processes, analyze administrative and internal systems needs, and facilitate and implements improvement methodologies to support compliance with federal/state/local/Company standards and achievement of operational and clinical goals.
In this role, the selected candidate will define and perform systems analysis and development tasks to improve workflow and operating efficiency; analyze costs of existing operations and prepares a cost/benefit analysis of recommended changes.