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The Company
Our client is in the top 5 largest pharma companies in the world, with locations all over the Netherlands. In their Leiden location, they mainly engage in the process of developing new vaccines for widespread diseases.

The Role
As a Study Administrator, you will support the clinical studies and assuring that the data they register is valid, accurate, and according to the laws and regulations. You will work in a multinational environment, with a team located all around the globe.

Your Responsibilities
- Manage the company's portfolio of clinical trials and studies
- Distribute and submit the study-related data and documents 
- Make sure that the data and documents meet quality standards and are in line with compliance norms
- Facilitate the public registration of data about the progress of the trial


Your Profile
- Degree in Business, Science, Technology, or any relevant fields
- + 3 years of experience in quality or in R&D 
- Experience in a highly regulated industry, such as Pharma, Chemicals, Biotechnology, etc.
- Fluent in English, other languages are a plus
- Solid knowledge of the Microsoft Office package
- Proactive mindset and good organizational skills

Other information
Are you ready for a new opportunity? This is your chance! If you are interested click the apply button bellow and I will get in contact with you as soon as possible.