As a RCTM at Boehringer Ingelheim you provide operational expertise to manage and oversee clinical trials conducted in different therapeutic areas that are under the management of the RCV office.
You supervise relationships with investigators, counsels Clinial Research Associates (CRAs) and Contract Research Organizations (CROs).
Furthermore you plan study budget, timelines and capacities and supervise monitoring activities and Co-Monitoring visits. Moreover you organize investigator meetings.

Requirements:

• medical doctor qualification or biological/natural science background
• profound experience as On-site Monitor (CRA) or Clinical Trial Manager
• good knowledge of international and national/regional guidelines and regulatory topics
• experience in project/trial management

Other job facts:

• language: English & German
• professional experience necessary: yes
• leading responsibilities: yes, trial based leadership
• project management responsibilities: yes