Registration Information Associate

Registration Information Associate with profound Regulatory Affairs knowledge wanted for our Basel based client in the pharmaceutical sector.

YOUR EXPERIENCE/SKILLS:

- 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

YOUR TASKS:

- 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

START: 05/2018

Duration: 08MM+

Location: Basel, Switzerland

Ref.Nr.: BH12725

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.

GOING THE EXTRA MILE.

NEW TO SWITZERLAND?

In case of successful placement, we support you with:

- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more