Registration Information Management Associate (NOVJP00026142) (m/f)

REFERENZNUMMER:

372009/11

IHRE AUFGABEN:

-With guidance, direct and monitor HQ and CO compliance with internal procedures governing registration information management activities at the global, regional and local level
-Expert in RA Systems (e.g. DRAGON) and related tools that support registration information management processes worldwide
-Provide counsel and guidance to RA CO colleagues regarding their accountability in the registration information process
-Support the regulatory strategy and contribute to the implementation of NovaRIM in collaboration with business owner and IT through e.g. data cleaning supervision on legacy systems (DRAGON, Sharepoint trackers, etc.), authoring of project-related documents etc.
-Support the achievement of consistent and sustainable performance against worldwide HA expectations and internal Novartis procedures governing registration information management

IHRE QUALIFIKATIONEN:

-BS or MS with requisite experience and demonstrated capability
-Fluency in English as a business language, additional language is an asset
-Previous experience mainly in a regulatory environmentClinical Development, GCP, QA)
-Understand and able to assist RA in understanding compliance and quality drivers from a global perspective
-Proven negotiation skills
-Demonstrated ability as a creative thinker
-Logical and methodical, with attention to details

WEITERE QUALIFIKATIONEN:

Project assistant