Function: You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures and the relevant regulations. You analyze and evaluate clinical data, ensure compliance with protocol and overall clinical objectives; identify, select, initiate and close-out appropriate investigational sites for clinical studies. You monitor the sites in order to ensure that studies are carried out according to the applicable regulations and guidelines. You act as mentor for junior staff members. Regular international travel is required.
Profile: By preference, you have a (para-) medical or scientific degree and at least three (3) years of clinical research experience (monitoring). You have excellent planning and organizational skills with good negotiation, time-management and people skills.
Fluent in German and English