Please provide your CV in English.

The scope of responsibilities will include:

• Constantly maintain and generate relations with Investigative Sites;
• Maintain and refine the internal site database in cooperation with Study Startup, Clinical Operations and Process Improvement;
• Participate in development of improvement strategies for the site identification process;
• Create the initial list of potential sites;
• Communicates with project teams to define strategy and methodology of initial and follow-up site contacts;
• In cooperation with the project team maintain a study site identification tracker;
• Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives;
• Perform due diligence check of regulatory limitations applicable to the recommended investigators or clinic...