* University degree with practical knowledge in the pharmaceutical or similar sector from outside Europe or US
* 3+ years' working experience in a regulatory environment or closely related areas like QA, Clinical Development and GCP
* Good Understanding and ability to assist RA as well as familiarity with compliance and quality drivers from a global perspective
* Competency of using IT systems and Expert in RA Systems and related tools that support registration information management processes
* Languages: fluent English both written and spoken
* Supporting regulatory strategy and implementation of processes and procedures to ensure sustained compliance with Health Authority regulations in collaboration with business owner and IT
* Performing data cleaning supervision on legacy systems like DRAGON or Sharepoint trackers along with maintaining the project-related documents
* Conducting and monitoring HQ and CO compliance with internal procedures governing registration information management activities and providing training as needed
* Providing counsel as well as guiding RA CO colleagues regarding their accountability in the registration information process
Location: Basel, Switzerland
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.
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