We are looking for a Clinical Manager to oversee Post-Authorisation Safety Studies across Europe for a successful biotechnology company specialising in treatments for Orphan Diseases.
This has been chosen as the job of the week as it is:
- A high profile role, interacting with Key Opinion Leaders in many countries.
- Responsible for ensuring the continued success of the company’s flagship product.
- An opportunity to become part of a highly innovative company, not afraid to challenge the established way of doing things.
- Offers a very competitive salary.