National Clinical Study Coordinator (60%)

Responsibilities:
Major tasks are the coordination of centers, supervision and continuous improvement of SOPs, monitoring of study centers and data quality, the maintenance of homepage, and communication with enrolled patients via newsletters and other relevant media forms.

Qualifications:
The candidate will have previous experience in the field of clinical studies/biobanking and documented knowledge of good clinical practice and ethical policies. Experience in leading studies at a national and international level is an advantage, as well as holding a CAS or DAS in clinical study management. The function requires excellent organizational skills to independently manage work flow and ability to prioritize quickly and appropriately.

As a national coordinator, you should speak and write German, English and French and show excellent communication skills, high competence in leading and motivating a team of study nurses located in five study centers, and interacting with the local medical investigators. Experience in the field of nutrition and/or epidemiology would be a bonus.

Language requirements:
English, German and French (written and spoken)

Computer skills:
The usual applications within clinical trial management

Special requirements:
Applications should be sent electronically and include a CV (incl. full publication list), copies of all relevant degrees, a statement of interest and reference letters.