Job openings

As the HR Officer responsible for the development and performance at Radiomics, you will be expected to assess the development needs to achieve the company goals, devise our organizational training strategy, drive its implementation and assess its outcomes.

As the Regulatory Affairs Manager, you will be responsible for the transition of the product from a development project to a marketed product in Life Cycle management (LCM). In addition, you will be overall RA responsible for the ongoing clinical trials, be involved in marketing authorization submissions in new countries as agreed within the QA and Commercial teams.

The Project Manager Pharma will work along with the Chief Scientific Officer (CSO) to make sure to deliver our results in such a way that they bring most value to the client.