The overall project management of German and international clinical studies,
Phase II-IV, in a range of therapeutic areas and you will have 3-5 years experience in a similar position in international clinical study management or extensive CRA experience in a CRO and/or in the pharmaceutical industry.
Experience in the UK/US market would be an advantage. You will have proven ability to lead and manage a project team and meeting study deadlines within budget, whilst maintaining quality standards and interacting well with sponsors, investigational site staff and in-house staff.
Being able to take the initiative and work independently is routine for you. Together with your team building and management skills.
Fluent in English and German, both spoken and written
