Clinical Study Administrator

CK Group are recruiting for a Clinical Trial Administrator to join a leading global pharmaceutical company based in Diegem, Belgium.

This individual will provide support to the clinical study staff within Clinical R&D, as well as fostering strong, productive relationships with colleagues within the Clinical R&D organisation.

Responsible for processing, tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required.

Education:

• Minimum of a Bachelor’s Degree is required.

Experience:

• Previous clinical research experience a plus.
• Requires previous administrative support experience or equivalent for at least 1 year.
• Clinical/medical background a plus.
• Speaking Dutch is required.
• Proven Flexibility and open to take some late meetings with the US around 7 PM.
• Available to work from Diegem, Belgium once a week.

Apply:

Please quote job reference 102873 in all correspondence.