|Publication date:||March 19 2021|
|Function Group:||Clinical Research|
For a fast growing and global Medical Devices company, we are looking for a Central Clinical Start-up Specialist on short notice for 20 hours per week (this can be flexible). The company is active on a global level and conducts clinical trials in 40 countries and in over 100 hospitals. For this role, you will be working home-based.
As a Central Clinical Start-up Specialist, you are responsible for the start-up, execution and closure activities of a clinical trial. You are aware of the legislations, policies and procedures and work according to these. In this role, you are the expert on the planning, preparations and execution of study submissions to the Ethics Committee. These submissions are your responsibility for the whole study.
You could also support other activities such as the clinical trials agreement process, submission to competent authorities, informed consent, translating study documents, facilitating meetings, working directly with sites for documentation etc.
The ideal candidate has:
The company offers:
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Senior Associate Quality & Clinical | Medical Devices