TFS is a Global CRO headquartered in Sweden. We genuinely believe that “Global in mind and local at heart” is the core of our success; we operate in a global environment while retaining an in-depth knowledge of regulatory requirements in every country where we operate. At TFS, you will be offered the possibility to develop in a global organization with a company culture distinguished by passion, innovation and talent.
Director Regulatory Affairs position is part of the Clincial Development Services organization supporting both the Centres of Excellence and the Study Startup groups.
It will provide TFS clients with expert input into the design and implementation of clinical development programs of pharmaceutical products and medical devices in the field of interest and the assigned therapeutic area.
Key Responsibilties:
Requirements
Benefits
What can we offer you?
A great place to work where you will get the chance to push your career to the next level, global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients.
We believe that a company with ethical and transparent values has a better chance of attracting skilled employees and building long-term relationships.